A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660397



Internal ID9579816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103014788..103014940hg38UCSC Ensembl
Outerchr9:103014751..103014990hg38UCSC Ensembl
Innerchr9:105777070..105777222hg19UCSC Ensembl
Outerchr9:105777033..105777272hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6101569, essv5842109, essv6014810, essv5548503, essv6107814, essv5980479, essv6462430, essv6034406, essv6370862, essv6301710, essv5656963, essv5775266, essv5442056, essv6379554, essv6430317, essv5726000, essv6026544, essv5561771, essv5978463, essv6337515, essv6187085, essv6098073, essv5476042, essv5417254, essv6408909, essv5853618, essv5545493, essv6347371, essv5554027, essv6319551, essv5490908, essv5663500, essv5713890, essv6316976, essv6360937, essv5451414, essv5671225, essv6403588
SamplesHG01441, HG00252, HG00619, NA18534, HG01072, HG00705, HG01173, HG00707, HG01389, HG00463, HG01082, HG01350, HG00581, HG00331, HG01375, HG00259, HG01061, HG00689, HG00315, HG00258, HG00284, HG00237, HG00436, HG00108, NA18620, HG00653, HG01170, HG01069, NA19704, HG00513, HG01070, HG00246, HG01334, NA18602, HG00281, HG01366, HG01374, HG00671
Known GenesCYLC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660397
Frequency
Sample Size1151
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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