A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13038342



Internal ID6621840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156165029..156165921hg38UCSC Ensembl
Innerchr7:156165040..156165910hg38UCSC Ensembl
Outerchr7:156165018..156165932hg38UCSC Ensembl
chr7:155957723..155958615hg19UCSC Ensembl
Innerchr7:155957734..155958604hg19UCSC Ensembl
Outerchr7:155957712..155958626hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615655
Supporting Variants
SamplesNA20786
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13038342
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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