A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155693



Internal ID15878230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149759270..149786285hg38UCSC Ensembl
Innerchr7:149456359..149483373hg19UCSC Ensembl
Innerchr7:149087292..149114306hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3827016
hg1927015
hg1827015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608985
Supporting Variants
SamplesHGDP01163
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155693
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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