A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6933



Internal ID15536930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:13647174..13654694hg38UCSC Ensembl
Outerchr20:13627821..13635341hg19UCSC Ensembl
Outerchr20:13575821..13583341hg18UCSC Ensembl
Outerchr20:13575821..13583341hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg386713
hg196713
hg186713
hg176713
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3294
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)nssv6933
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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