A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9094



Internal ID15534770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:21734842..21769003hg38UCSC Ensembl
Outerchr13:22308981..22343142hg19UCSC Ensembl
Outerchr13:21206981..21241142hg18UCSC Ensembl
Outerchr13:21206981..21241142hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg385263
hg195263
hg185263
hg175263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956
Supporting Variants
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)nssv9094
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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