A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769168



Internal ID18964968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5804988..5805289hg38UCSC Ensembl
chr19:5804999..5805300hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072311
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769168
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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