A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959121



Internal ID18857914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:60100..82500hg38UCSC Ensembl
Outerchr19:60100..82500hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3822401
hg1922401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118608
Supporting Variants
SamplesKWS1
Known GenesFAM138A, FAM138F, WASH5P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959121
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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