A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3342



Internal ID15547942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:25613217..25646797hg38UCSC Ensembl
Outerchr20:25593853..25627433hg19UCSC Ensembl
Outerchr20:25541853..25575433hg18UCSC Ensembl
Outerchr20:25541853..25575433hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg387418
hg197418
hg187418
hg177418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1595
SamplesNA19240
Known GenesNANP
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)nsv3342
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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