A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658662



Internal ID9924767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110508312..110512254hg38UCSC Ensembl
Outerchr7:110508155..110512407hg38UCSC Ensembl
Innerchr7:110148369..110152311hg19UCSC Ensembl
Outerchr7:110148212..110152464hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg384253
hg194253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6472879, essv5832101, essv6083963
SamplesNA19651, NA20812, HG00326
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658662
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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