A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10659



Internal ID15542139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42720813..42752045hg38UCSC Ensembl
Outerchr9:44219074..44250306hg19UCSC Ensembl
Outerchr9:44159070..44190302hg18UCSC Ensembl
Outerchr9:43370147..43401379hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388276
hg198276
hg188276
hg178276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541
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)nssv10659
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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