A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155928



Internal ID15529450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155389631..155420948hg38UCSC Ensembl
Innerchr7:155182326..155213643hg19UCSC Ensembl
Innerchr7:154875087..154906404hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3831318
hg1931318
hg1831318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609161
Supporting Variants
SamplesHGDP00788
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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