A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11041



Internal ID15539667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63675224..63696350hg38UCSC Ensembl
Outerchr20:62306577..62327703hg19UCSC Ensembl
Outerchr20:61777021..61798147hg18UCSC Ensembl
Outerchr20:61777021..61798147hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810011
hg1910011
hg1810011
hg1710011
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3449
Supporting Variants
SamplesNA15510
Known GenesRTEL1, RTEL1-TNFRSF6B
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)nssv11041
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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