A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10006



Internal ID15542791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:112296592..112307118hg38UCSC Ensembl
Outerchr13:112950906..112961432hg19UCSC Ensembl
Outerchr13:111998907..112009433hg18UCSC Ensembl
Outerchr13:111998907..112009433hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3810527
hg1910527
hg1810527
hg1710527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1189
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)nssv10006
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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