A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625065



Internal ID21817112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4572543..4578011hg38UCSC Ensembl
chr19:4572555..4578023hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385469
hg195469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625065
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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