A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657098



Internal ID9923203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16039944..16062449hg38UCSC Ensembl
chr1:16366439..16388944hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3822506
hg1922506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv20e199
Supporting Variantsessv5962586, essv6332122, essv6480939, essv6164946, essv5865210, essv6336747, essv5437805, essv6522112, essv5666576, essv6255300, essv6157232, essv6017997, essv6042600, essv6563266, essv5721205, essv6389354, essv6230246, essv5874963, essv6472652, essv5737844, essv6570595, essv5801977, essv5473940, essv5946173, essv5521239, essv6508179, essv6502464, essv5647330, essv6512268, essv5910818, essv5830282, essv6041952, essv6139377, essv5667798, essv5946084, essv5864888, essv6252837, essv6475130, essv5519523, essv5868013
SamplesNA20761, HG00650, HG00542, NA19058, HG00671, NA18561, HG01066, HG00566, HG01518, NA18988, NA19660, NA18940, NA18567, NA18960, NA18574, NA18582, NA19782, NA18964, HG00590, NA18977, HG00326, NA11831, HG01136, HG00443, NA20770, HG01390, NA18573, HG00531, HG00613, NA20828, NA19072, NA19010, NA19360, HG00656, HG01254, NA19661, NA19004, NA19758, HG00171, NA18620
Known GenesCLCNKB, FAM131C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657098
Frequency
Sample Size1151
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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