A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9413



Internal ID15540364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:150816994..150850280hg38UCSC Ensembl
Outerchr5:150196556..150229842hg19UCSC Ensembl
Outerchr5:150176749..150210035hg18UCSC Ensembl
Outerchr5:150176749..150210035hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3833287
hg1933287
hg1833287
hg1733287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5067
Supporting Variants
SamplesNA18517
Known GenesIRGM
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)nssv9413
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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