A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6949



Internal ID15536914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63684160..63694846hg38UCSC Ensembl
Outerchr20:62315513..62326199hg19UCSC Ensembl
Outerchr20:61785957..61796643hg18UCSC Ensembl
Outerchr20:61785957..61796643hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg389317
hg199317
hg189317
hg179317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3449
Supporting Variants
SamplesNA12156
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)nssv6949
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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