A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026569



Internal ID19115787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30419932..30564987hg38UCSC Ensembl
Innerchr9:30419930..30564985hg19UCSC Ensembl
Innerchr9:30409930..30554985hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38145056
hg19145056
hg18145056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7504n100
Supporting Variantsnssv3688822
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)nsv1026569
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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