A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626553



Internal ID6666703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60174821..60175219hg38UCSC Ensembl
Innerchr11:60174821..60175219hg38UCSC Ensembl
Outerchr11:60174525..60175529hg38UCSC Ensembl
chr11:59942294..59942692hg19UCSC Ensembl
Innerchr11:59942294..59942692hg19UCSC Ensembl
Outerchr11:59941998..59943002hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14174925, essv14174922, essv14174942, essv14174916, essv14174952, essv14174926, essv14174931, essv14174941, essv14174950, essv14174949, essv14174947, essv14174935, essv14174929, essv14174923, essv14174921, essv14174943, essv14174918, essv14174930, essv14174944, essv14174919, essv14174937, essv14174924, essv14174946, essv14174954, essv14174940, essv14174920, essv14174927, essv14174938, essv14174932, essv14174953, essv14174936, essv14174928, essv14174951, essv14174934, essv14174933, essv14174939, essv14174945, essv14174917, essv14174948
SamplesHG02386, HG02262, HG02150, HG02078, NA18486, HG03229, HG02154, NA19746, HG00599, NA18567, HG00458, HG00379, HG02067, NA19731, HG01849, HG01275, NA18638, HG01136, NA19056, HG00360, NA18630, HG01049, HG01921, HG00525, NA18963, HG01572, HG01977, HG01933, NA18643, NA18943, HG00672, HG00409, NA19726, HG03162, HG01377, HG00595, HG01125, HG01578, HG00593
Known GenesMS4A6A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626553
Frequency
Sample Size2504
Observed Gain0
Observed Loss39
Observed Complex0
Frequencyn/a


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