A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620958



Internal ID21813005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3891196..3893176hg38UCSC Ensembl
chr19:3891194..3893174hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049220
Supporting Variants
Samples
Known GenesATCAY
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620958
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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