A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692019



Internal ID18990300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27285644..27300320hg38UCSC Ensembl
Innerchr9:27285642..27300318hg19UCSC Ensembl
Innerchr9:27275642..27290318hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3814677
hg1914677
hg1814677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020925
Supporting Variants
Samples
Known GenesEQTN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3692019
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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