A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988286



Internal ID19220767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:66214375..66240898hg38UCSC Ensembl
Outerchr4:67080093..67106616hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3826524
hg1926524
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133342
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988286
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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