A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6442609



Internal ID9636462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109522478..109523961hg38UCSC Ensembl
Outerchr7:109522441..109524011hg38UCSC Ensembl
Innerchr7:109162535..109164018hg19UCSC Ensembl
Outerchr7:109162498..109164068hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666077
Supporting Variants
SamplesNA19372
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6442609
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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