A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3693152



Internal ID18991433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61612691hg38UCSC Ensembl
Innerchr9:44727847..44820529hg19UCSC Ensembl
Innerchr9:44667843..44760525hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3892683
hg1992683
hg1892683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027504
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)nssv3693152
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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