A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10286



Internal ID15195826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:20051215..20083522hg38UCSC Ensembl
Outerchr20:20031859..20064166hg19UCSC Ensembl
Outerchr20:19979859..20012166hg18UCSC Ensembl
Outerchr20:19979859..20012166hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg387203
hg197203
hg187203
hg177203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3320
Supporting Variants
SamplesNA18956
Known GenesC20orf26, CRNKL1
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)nssv10286
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer