A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6940



Internal ID15190238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:33726971..33759820hg38UCSC Ensembl
Outerchr20:32314777..32347626hg19UCSC Ensembl
Outerchr20:31778438..31811287hg18UCSC Ensembl
Outerchr20:31778438..31811287hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg386588
hg196588
hg186588
hg176588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3355
Supporting Variants
SamplesNA12156
Known GenesZNF341
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)nssv6940
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer