A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608979



Internal ID16396388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149700974..149765532hg38UCSC Ensembl
Innerchr7:149398065..149462621hg19UCSC Ensembl
Innerchr7:149028998..149093554hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3864559
hg1964557
hg1864557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1099471
Samples
Known GenesKRBA1, ZNF467
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608979
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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