A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8152



Internal ID15535712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:133720885..133765720hg38UCSC Ensembl
Outerchr5:133056576..133101411hg19UCSC Ensembl
Outerchr5:133084475..133129310hg18UCSC Ensembl
Outerchr5:133084475..133129310hg17UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3844836
hg1944836
hg1844836
hg1744836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5008
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)nssv8152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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