A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021134



Internal ID19110352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24285432..24342625hg38UCSC Ensembl
Innerchr9:24285430..24342623hg19UCSC Ensembl
Innerchr9:24275430..24332623hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3857194
hg1957194
hg1857194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690745
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)nsv1021134
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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