A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10337



Internal ID15542461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:37495377..37521210hg38UCSC Ensembl
Outerchr3:37536868..37562701hg19UCSC Ensembl
Outerchr3:37511872..37537705hg18UCSC Ensembl
Outerchr3:37511872..37537705hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg387569
hg197569
hg187569
hg177569
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3763
Supporting Variants
SamplesNA18956
Known GenesITGA9
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)nssv10337
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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