A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656996



Internal ID9923101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3297439..3297758hg38UCSC Ensembl
chr17:3200733..3201052hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6201747, essv6346188, essv5746680, essv5551484, essv6279485, essv5484779, essv6150761, essv5927682, essv5436060, essv5649310, essv6027365, essv5829194, essv5730202, essv5582249, essv5936701, essv5640140, essv5448694, essv5608654, essv5972101, essv5850277, essv6549746, essv5609650, essv6596726, essv6215550, essv6063040, essv5581514
SamplesNA18507, NA19359, NA18486, NA18545, NA19190, NA18870, NA18582, NA19383, NA11994, NA18605, NA19210, NA19455, NA18579, NA19114, NA18499, NA18912, NA18858, NA19834, NA19108, NA19434, NA18564, NA19360, NA19398, NA19102, NA19129, NA12776
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656996
Frequency
Sample Size1151
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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