A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11113



Internal ID15539466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:156033774..156073476hg38UCSC Ensembl
Outerchr5:155460784..155500486hg19UCSC Ensembl
Outerchr5:155393362..155433064hg18UCSC Ensembl
Outerchr5:155393362..155433064hg17UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3839703
hg1939703
hg1839703
hg1739703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5087
Supporting Variants
SamplesNA15510
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)nssv11113
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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