A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964034



Internal ID19219576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:28922219..28922275hg38UCSC Ensembl
Outerchr4:28923841..28923897hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129725
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964034
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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