A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690602



Internal ID18988883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13008543..13064794hg38UCSC Ensembl
Innerchr9:13008542..13064793hg19UCSC Ensembl
Innerchr9:12998542..13054793hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3856252
hg1956252
hg1856252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023816
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)nssv3690602
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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