A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962064



Internal ID19225177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:1026082..1026287hg38UCSC Ensembl
Outerchr4:1019870..1020075hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120469
Supporting Variants
SamplesKWS1
Known GenesFGFRL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962064
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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