A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7815



Internal ID15189363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:63632791..63666859hg38UCSC Ensembl
Outerchr3:63618467..63652535hg19UCSC Ensembl
Outerchr3:63593507..63627575hg18UCSC Ensembl
Outerchr3:63593507..63627575hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg385369
hg195369
hg185369
hg175369
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3849
Supporting Variants
SamplesNA12156
Known GenesSNTN
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)nssv7815
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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