A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755938



Internal ID19054219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38736900..38771834hg38UCSC Ensembl
Innerchr9:38736897..38771831hg19UCSC Ensembl
Innerchr9:38726897..38761831hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3834935
hg1934935
hg1834935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020969
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)nssv3755938
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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