A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4632



Internal ID15543319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:103922151..103966603hg38UCSC Ensembl
Outerchr13:104574501..104618953hg19UCSC Ensembl
Outerchr13:103372502..103416954hg18UCSC Ensembl
Outerchr13:103372502..103416954hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3844453
hg1944453
hg1844453
hg1744453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1162
Supporting Variants
SamplesNA19129
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)nssv4632
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer