A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625151



Internal ID21817198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:581025..581094hg38UCSC Ensembl
chr19:581025..581094hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038130
Supporting Variants
Samples
Known GenesBSG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625151
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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