A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692360



Internal ID18990641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2255397..2410590hg38UCSC Ensembl
Innerchr9:2255397..2410590hg19UCSC Ensembl
Innerchr9:2245397..2400590hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38155194
hg19155194
hg18155194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016401
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)nssv3692360
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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