A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9415



Internal ID15540366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:156036531..156078120hg38UCSC Ensembl
Outerchr5:155463541..155505130hg19UCSC Ensembl
Outerchr5:155396119..155437708hg18UCSC Ensembl
Outerchr5:155396119..155437708hg17UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3841590
hg1941590
hg1841590
hg1741590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5087
Supporting Variants
SamplesNA18517
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)nssv9415
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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