A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2899



Internal ID15541658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:31547861..31581542hg38UCSC Ensembl
Outerchr13:32121998..32155679hg19UCSC Ensembl
Outerchr13:31019998..31053679hg18UCSC Ensembl
Outerchr13:31019998..31053679hg17UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg386334
hg196334
hg186334
hg176334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv987
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)nssv2899
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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