A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979860



Internal ID19241121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:67398494..67401070hg38UCSC Ensembl
Outerchr4:68264212..68266788hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg382577
hg192577
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143094
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979860
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