A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022674



Internal ID19111892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26453725..26668104hg38UCSC Ensembl
Innerchr9:26453723..26668102hg19UCSC Ensembl
Innerchr9:26443723..26658102hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38214380
hg19214380
hg18214380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7485n100
Supporting Variantsnssv3692000
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)nsv1022674
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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