A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9990



Internal ID15195221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:46446748..46474764hg38UCSC Ensembl
Outerchr13:47020883..47048899hg19UCSC Ensembl
Outerchr13:45918884..45946900hg18UCSC Ensembl
Outerchr13:45918884..45946900hg17UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3828017
hg1928017
hg1828017
hg1728017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1025
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)nssv9990
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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