A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618078



Internal ID21810125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50866001..50866686hg38UCSC Ensembl
chr19:51369257..51369942hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044313
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618078
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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