A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993890



Internal ID19242019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:7561511..7561714hg38UCSC Ensembl
Outerchr4:7563238..7563441hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142383
Supporting Variants
SamplesKWS2
Known GenesSORCS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993890
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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