A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657380



Internal ID9923485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:145571646..145572037hg38UCSC Ensembl
Outerchr7:145571489..145572190hg38UCSC Ensembl
Innerchr7:145268739..145269130hg19UCSC Ensembl
Outerchr7:145268582..145269283hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6569326, essv6344795, essv5833937, essv5813062, essv5662573, essv6503615
SamplesNA19332, NA19359, NA19404, NA19099, HG01489, NA19093
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657380
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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