A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634763



Internal ID7021564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65120830..65126216hg38UCSC Ensembl
Innerchr14:65120980..65126066hg38UCSC Ensembl
Outerchr14:65120680..65126366hg38UCSC Ensembl
chr14:65587548..65592934hg19UCSC Ensembl
Innerchr14:65587698..65592784hg19UCSC Ensembl
Outerchr14:65587398..65593084hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg385387
hg195387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15042954, essv15042956, essv15042966, essv15042973, essv15042951, essv15042962, essv15042971, essv15042969, essv15042964, essv15042970, essv15042959, essv15042961, essv15042953, essv15042955, essv15042957, essv15042952, essv15042967, essv15042960, essv15042974, essv15042958, essv15042968, essv15042963, essv15042965, essv15042972, essv15042975
SamplesHG02610, NA19204, NA19819, HG02624, NA20589, NA19131, NA19130, NA19922, NA19917, HG01950, NA19327, NA18915, HG02508, NA19042, NA19318, HG03354, HG01956, HG03567, HG02721, HG03084, NA19468, HG03401, NA19312, HG03376, HG01886
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634763
Frequency
Sample Size2504
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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