A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608985



Internal ID16396394
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 StatusM
Merged Variantsdgv11716n54
Supporting Variantsnssv1155693
SamplesHGDP01163
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608985
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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