A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9298



Internal ID15540249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:112277120..112298605hg38UCSC Ensembl
Outerchr13:112931434..112952919hg19UCSC Ensembl
Outerchr13:111979435..112000920hg18UCSC Ensembl
Outerchr13:111979435..112000920hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3821486
hg1921486
hg1821486
hg1721486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1189
Supporting Variants
SamplesNA18517
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)nssv9298
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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