A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615651



Internal ID7002540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156126614..156127065hg38UCSC Ensembl
Innerchr7:156126619..156127061hg38UCSC Ensembl
Outerchr7:156126610..156127070hg38UCSC Ensembl
chr7:155919308..155919759hg19UCSC Ensembl
Innerchr7:155919313..155919755hg19UCSC Ensembl
Outerchr7:155919304..155919764hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13038325, essv13038328, essv13038331, essv13038330, essv13038329, essv13038324, essv13038320, essv13038326, essv13038321, essv13038322, essv13038327, essv13038323
SamplesHG00143, HG01676, HG00129, HG00346, NA20535, NA19908, HG03054, HG01936, NA19773, HG00237, HG01111, NA20754
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615651
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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