A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632563



Internal ID21824610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5528698..5547643hg38UCSC Ensembl
chr19:5528709..5547654hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3818946
hg1918946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052266
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632563
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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