A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962071



Internal ID19211529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:14833939..14834065hg38UCSC Ensembl
Outerchr4:14835563..14835689hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120474
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962071
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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