A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689113



Internal ID18987394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7735724..7770825hg38UCSC Ensembl
Innerchr9:7735724..7770825hg19UCSC Ensembl
Innerchr9:7725724..7760825hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3835102
hg1935102
hg1835102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022474
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689113
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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