A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026376



Internal ID19115594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30784558..30817070hg38UCSC Ensembl
Innerchr9:30784556..30817068hg19UCSC Ensembl
Innerchr9:30774556..30807068hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3832513
hg1932513
hg1832513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688841
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)nsv1026376
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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