A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10651



Internal ID15542147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:5470916..5496713hg38UCSC Ensembl
Outerchr9:5470916..5496713hg19UCSC Ensembl
Outerchr9:5460916..5486713hg18UCSC Ensembl
Outerchr9:5460916..5486713hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg387547
hg197547
hg187547
hg177547
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6461
Supporting Variants
SamplesNA18956
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)nssv10651
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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