A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613262



Internal ID16400671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7336443..7417689hg38UCSC Ensembl
Innerchr9:7336443..7417689hg19UCSC Ensembl
Innerchr9:7326443..7407689hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3881247
hg1981247
hg1881247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126852
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613262
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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