A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027996



Internal ID19117214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31164391..31568048hg38UCSC Ensembl
Innerchr9:31164389..31568046hg19UCSC Ensembl
Innerchr9:31154389..31558046hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38403658
hg19403658
hg18403658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7510n100
Supporting Variantsnssv3688847
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)nsv1027996
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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