A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9104



Internal ID15534760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:31525457..31557581hg38UCSC Ensembl
Outerchr13:32099594..32131718hg19UCSC Ensembl
Outerchr13:30997594..31029718hg18UCSC Ensembl
Outerchr13:30997594..31029718hg17UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3832125
hg1932125
hg1832125
hg1732125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv986
Supporting Variants
SamplesNA12156
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)nssv9104
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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