A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10281



Internal ID15542517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:4428765..4452607hg38UCSC Ensembl
Outerchr20:4409412..4433254hg19UCSC Ensembl
Outerchr20:4357412..4381254hg18UCSC Ensembl
Outerchr20:4357412..4381254hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387101
hg197101
hg187101
hg177101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3267
Supporting Variants
SamplesNA18956
Known Genes
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)nssv10281
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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