A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1799



Internal ID15541082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:113710186..113743292hg38UCSC Ensembl
Outerchr9:116472466..116505572hg19UCSC Ensembl
Outerchr9:115512287..115545393hg18UCSC Ensembl
Outerchr9:113552020..113585126hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386912
hg196912
hg186912
hg176912
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6675
Supporting Variants
SamplesNA18555
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)nssv1799
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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