A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3360



Internal ID15201276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34562312..34597446hg38UCSC Ensembl
Outerchr20:33150116..33185250hg19UCSC Ensembl
Outerchr20:32613777..32648911hg18UCSC Ensembl
Outerchr20:32613777..32648911hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg385868
hg195868
hg185868
hg175868
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1598
SamplesNA19240
Known GenesPIGU
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)nsv3360
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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