A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13038314



Internal ID2126394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156089668..156094157hg38UCSC Ensembl
Innerchr7:156089668..156094157hg38UCSC Ensembl
Outerchr7:156089290..156094430hg38UCSC Ensembl
chr7:155882362..155886851hg19UCSC Ensembl
Innerchr7:155882362..155886851hg19UCSC Ensembl
Outerchr7:155881984..155887124hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384490
hg194490
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615650
Supporting Variants
SamplesHG01932
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13038314
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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