A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979408



Internal ID18900572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:44963303..44963383hg38UCSC Ensembl
Outerchr19:45466560..45466640hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117220
Supporting Variants
SamplesKWS2
Known GenesCLPTM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979408
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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