A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016764



Internal ID19105981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1564704..1736070hg38UCSC Ensembl
Innerchr9:1564704..1736070hg19UCSC Ensembl
Innerchr9:1554704..1726070hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38171367
hg19171367
hg18171367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692351
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)nsv1016764
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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