A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461



Internal ID15551373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:5470916..5500311hg38UCSC Ensembl
Outerchr9:5470916..5500311hg19UCSC Ensembl
Outerchr9:5460916..5490311hg18UCSC Ensembl
Outerchr9:5460916..5490311hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg386817
hg196817
hg186817
hg176817
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6264, nssv10651
SamplesNA12156, NA18956
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv6461
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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