A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690645



Internal ID18988926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17049322..17081685hg38UCSC Ensembl
Innerchr9:17049320..17081683hg19UCSC Ensembl
Innerchr9:17039320..17071683hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3832364
hg1932364
hg1832364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019424
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)nssv3690645
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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