A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2758595



Internal ID17833628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9638876..9662703hg38UCSC Ensembl
Innerchr11:9660423..9684250hg19UCSC Ensembl
Innerchr11:9616999..9640826hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3823828
hg1923828
hg1823828
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972945
Supporting Variants
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2758595
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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