A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5158



Internal ID15549939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:179519890..179541476hg38UCSC Ensembl
Outerchr5:178946891..178968477hg19UCSC Ensembl
Outerchr5:178879497..178901083hg18UCSC Ensembl
Outerchr5:178879497..178901083hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3821587
hg1921587
hg1821587
hg1721587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8206
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)nsv5158
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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