A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027298



Internal ID19116517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24644780..24764076hg38UCSC Ensembl
Innerchr9:24644778..24764074hg19UCSC Ensembl
Innerchr9:24634778..24754074hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38119297
hg19119297
hg18119297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690848
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)nsv1027298
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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