A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959634



Internal ID19206215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:175918697..175941297hg38UCSC Ensembl
Outerchr5:175345700..175368300hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3822601
hg1922601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118740
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959634
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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