A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993858



Internal ID18888898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:20061998..20062096hg38UCSC Ensembl
Outerchr3:20103490..20103588hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142354
Supporting Variants
SamplesKWS2
Known GenesKAT2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993858
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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