A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976769



Internal ID15924039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151793297..151864407hg38UCSC Ensembl
Innerchr3:151511085..151582195hg19UCSC Ensembl
Innerchr3:152993775..153064885hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3871111
hg1971111
hg1871111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592051
Supporting Variants
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976769
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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