A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962060



Internal ID19217905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:189501071..189501155hg38UCSC Ensembl
Outerchr3:189218860..189218944hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120467
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962060
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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