A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755906



Internal ID19054187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29898400..29934465hg38UCSC Ensembl
Innerchr9:29898398..29934463hg19UCSC Ensembl
Innerchr9:29888398..29924463hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3836066
hg1936066
hg1836066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023159
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)nssv3755906
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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