A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656872



Internal ID9922977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38639778..38640772hg38UCSC Ensembl
chr17:36796031..36797025hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6445379, essv6582203, essv5415488, essv5404057, essv6223139, essv6235101, essv6065216, essv6080049, essv5662553, essv5685932, essv5769144, essv5977871, essv5854930, essv5507184, essv5862017, essv5467512, essv6496062, essv5521658, essv5839388, essv5980054, essv6342002, essv5456453, essv5684616, essv5887885, essv5789964, essv5887440, essv5685618, essv5673404, essv6017640, essv5929207
SamplesNA19058, NA20766, NA19066, HG01052, NA19819, NA19920, NA19067, NA20769, NA18574, NA19313, NA18874, NA18868, NA19189, NA19056, NA19717, NA19654, NA11893, HG00525, HG00258, NA19834, HG01375, NA19679, HG00131, NA11843, NA19900, NA19661, NA18488, NA20585, NA18487, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656872
Frequency
Sample Size1151
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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