A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022289



Internal ID19111507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26453725..26670585hg38UCSC Ensembl
Innerchr9:26453723..26670583hg19UCSC Ensembl
Innerchr9:26443723..26660583hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38216861
hg19216861
hg18216861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7485n100
Supporting Variantsnssv3692002
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)nsv1022289
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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