A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689121



Internal ID18987402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8223541..8303017hg38UCSC Ensembl
Innerchr9:8223541..8303017hg19UCSC Ensembl
Innerchr9:8213541..8293017hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3879477
hg1979477
hg1879477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016723
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)nssv3689121
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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