A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769619



Internal ID19308121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:49231682..49294583hg38UCSC Ensembl
chr4:49233699..49296600hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3862902
hg1962902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077968
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769619
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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