A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764332



Internal ID18961431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:603799..605100hg38UCSC Ensembl
chr19:603799..605100hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071484
Supporting Variants
SamplesKWP1
Known GenesHCN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764332
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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