A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156107



Internal ID15508207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158891461..159127494hg38UCSC Ensembl
Innerchr7:158684152..158920185hg19UCSC Ensembl
Innerchr7:158376913..158612946hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38236034
hg19236034
hg18236034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609422
Supporting Variants
Samples1780862379_A
Known GenesLINC00689, VIPR2, WDR60
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156107
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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