A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614648



Internal ID6654853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113470094..113470894hg38UCSC Ensembl
Innerchr7:113470151..113470837hg38UCSC Ensembl
Outerchr7:113470037..113470951hg38UCSC Ensembl
chr7:113110149..113110949hg19UCSC Ensembl
Innerchr7:113110206..113110892hg19UCSC Ensembl
Outerchr7:113110092..113111006hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12931443
SamplesNA19834
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614648
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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