A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992883



Internal ID19243051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:25752564..25777864hg38UCSC Ensembl
Outerchr20:25733200..25758500hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3825301
hg1925301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141380
Supporting Variants
SamplesKWS2
Known GenesFAM182B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992883
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