A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976762



Internal ID15924032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151792469..151875430hg38UCSC Ensembl
Innerchr3:151510257..151593218hg19UCSC Ensembl
Innerchr3:152992947..153075908hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3882962
hg1982962
hg1882962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592048
Supporting Variants
Samples
Known GenesAADAC, MIR548H2, SUCNR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976762
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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