A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10287



Internal ID15195825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:21126749..21129964hg38UCSC Ensembl
Outerchr20:21107390..21110605hg19UCSC Ensembl
Outerchr20:21055390..21058605hg18UCSC Ensembl
Outerchr20:21055390..21058605hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg386983
hg196983
hg186983
hg176983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3326
Supporting Variants
SamplesNA18956
Known GenesPLK1S1
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)nssv10287
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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