A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963346



Internal ID19210297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:176807741..176807833hg38UCSC Ensembl
Outerchr4:177728895..177728987hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111285
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963346
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