A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720962



Internal ID144628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6801856..6801921hg38UCSC Ensembl
chr19:6801867..6801932hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527260
Supporting Variants
Samples
Known GenesVAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720962
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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