A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5865



Internal ID15543525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:5743400..5776932hg38UCSC Ensembl
Outerchr20:5724046..5757578hg19UCSC Ensembl
Outerchr20:5672046..5705578hg18UCSC Ensembl
Outerchr20:5672046..5705578hg17UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg385751
hg195751
hg185751
hg175751
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3270
Supporting Variants
SamplesNA19129
Known GenesC20orf196
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)nssv5865
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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