A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628074



Internal ID21820121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7598665..7599050hg38UCSC Ensembl
chr19:7663551..7663936hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047998
Supporting Variants
Samples
Known GenesCAMSAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628074
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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