A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9105



Internal ID15534759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:33217381..33262567hg38UCSC Ensembl
Outerchr13:33791518..33836704hg19UCSC Ensembl
Outerchr13:32689518..32734704hg18UCSC Ensembl
Outerchr13:32689518..32734704hg17UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3845187
hg1945187
hg1845187
hg1745187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv991
Supporting Variants
SamplesNA12156
Known GenesSTARD13
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)nssv9105
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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