A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962477



Internal ID19215034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:43622688..43622744hg38UCSC Ensembl
Outerchr20:42251328..42251384hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111211
Supporting Variants
SamplesKWS1
Known GenesIFT52
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962477
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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