A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637843



Internal ID6677943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8732186..8733864hg38UCSC Ensembl
Innerchr16:8732187..8733863hg38UCSC Ensembl
Outerchr16:8732185..8733865hg38UCSC Ensembl
chr16:8826043..8827721hg19UCSC Ensembl
Innerchr16:8826044..8827720hg19UCSC Ensembl
Outerchr16:8826042..8827722hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381679
hg191679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15371951, essv15371925, essv15371982, essv15371947, essv15371995, essv15371972, essv15371940, essv15371942, essv15371962, essv15371969, essv15371950, essv15371927, essv15371932, essv15371949, essv15371957, essv15371933, essv15371996, essv15371987, essv15371992, essv15371960, essv15371980, essv15371968, essv15371989, essv15371994, essv15371938, essv15371986, essv15371941, essv15371965, essv15371978, essv15371935, essv15371934, essv15371946, essv15371975, essv15371983, essv15371963, essv15371981, essv15371926, essv15371967, essv15371988, essv15371977, essv15371936, essv15371959, essv15371984, essv15371943, essv15371971, essv15371931, essv15371954, essv15371985, essv15371930, essv15371928, essv15371961, essv15371964, essv15371979, essv15371991, essv15371944, essv15371953, essv15371922, essv15371924, essv15371970, essv15371937, essv15371966, essv15371952, essv15371976, essv15371974, essv15371958, essv15371973, essv15371923, essv15371993, essv15371956, essv15371955, essv15371945, essv15371990, essv15371929, essv15371948, essv15371939
SamplesHG03163, NA19137, NA19913, NA19214, NA18520, NA19904, HG03521, NA18871, HG02255, HG03086, HG02419, NA20294, HG03313, NA18516, HG02952, HG01956, HG03046, NA18517, HG03124, HG01883, NA20321, HG01049, NA19461, NA19144, NA19108, HG02976, NA19143, NA20320, NA19984, NA19323, NA19020, HG02577, HG02703, NA19908, NA20282, HG03114, NA19380, NA19189, HG02449, HG02537, NA19206, HG03455, NA19027, NA18486, NA18510, NA19119, HG03472, NA19901, HG02938, HG01889, HG02502, HG02307, HG01894, NA19711, HG03118, HG02624, HG03132, HG01971, NA19452, HG03139, HG03270, HG03060, NA19095, NA19171, HG03372, NA18853, HG02798, NA19113, NA19350, HG02813, HG02013, HG01890, NA18519, HG03095, HG02610
Known GenesABAT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637843
Frequency
Sample Size2504
Observed Gain0
Observed Loss75
Observed Complex0
Frequencyn/a


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