A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984030



Internal ID18898811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:168155741..168157697hg38UCSC Ensembl
Outerchr4:169076892..169078848hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381957
hg191957
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125827
Supporting Variants
SamplesKWS2
Known GenesANXA10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984030
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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