A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1666



Internal ID15545399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:33723105..33755391hg38UCSC Ensembl
Outerchr3:33764597..33796883hg19UCSC Ensembl
Outerchr3:33739601..33771887hg18UCSC Ensembl
Outerchr3:33739601..33771887hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg388712
hg198712
hg188712
hg178712
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3757
Supporting Variants
SamplesNA19240
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)nssv1666
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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