A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022029



Internal ID19111247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29898400..29976361hg38UCSC Ensembl
Innerchr9:29898398..29976359hg19UCSC Ensembl
Innerchr9:29888398..29966359hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3877962
hg1977962
hg1877962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755907
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)nsv1022029
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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