A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6924



Internal ID15190254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1869698..1887163hg38UCSC Ensembl
Outerchr20:1850344..1867809hg19UCSC Ensembl
Outerchr20:1798344..1815809hg18UCSC Ensembl
Outerchr20:1798344..1815809hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3813049
hg1913049
hg1813049
hg1713049
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3257
Supporting Variants
SamplesNA12156
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)nssv6924
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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