A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3731



Internal ID15201684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:23173270..23207099hg38UCSC Ensembl
Outerchr3:23214761..23248590hg19UCSC Ensembl
Outerchr3:23189765..23223594hg18UCSC Ensembl
Outerchr3:23189765..23223594hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385610
hg195610
hg185610
hg175610
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7777
SamplesNA12156
Known GenesUBE2E2
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)nsv3731
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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