A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992938



Internal ID19232179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:65510625..65513725hg38UCSC Ensembl
Outerchr3:65496300..65499400hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg383101
hg193101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141433
Supporting Variants
SamplesKWS2
Known GenesMAGI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992938
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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