A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9354



Internal ID15540305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:146082018..146121198hg38UCSC Ensembl
Outerchr2:146839586..146878766hg19UCSC Ensembl
Outerchr2:146556056..146595236hg18UCSC Ensembl
Outerchr2:146673318..146712498hg17UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3839181
hg1939181
hg1839181
hg1739181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2960
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)nssv9354
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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