A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137



Internal ID15199014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:97151220..97196560hg38UCSC Ensembl
Outerchr13:97803474..97848814hg19UCSC Ensembl
Outerchr13:96601475..96646815hg18UCSC Ensembl
Outerchr13:96601475..96646815hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3845341
hg1945341
hg1845341
hg1745341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6574
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)nsv1137
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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