A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962



Internal ID15552983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:23642052..23688036hg38UCSC Ensembl
Outerchr13:24216191..24262175hg19UCSC Ensembl
Outerchr13:23114191..23160175hg18UCSC Ensembl
Outerchr13:23114191..23160175hg17UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3845985
hg1945985
hg1845985
hg1745985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6551
SamplesNA12156
Known GenesTNFRSF19
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)nsv962
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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