A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755835



Internal ID19054116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21196301..21269670hg38UCSC Ensembl
Innerchr9:21196300..21269669hg19UCSC Ensembl
Innerchr9:21186300..21259669hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3873370
hg1973370
hg1873370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035128
Supporting Variants
Samples
Known GenesIFNA10, IFNA14, IFNA16, IFNA17, IFNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755835
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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