A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625659



Internal ID21817706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38297040..38297646hg38UCSC Ensembl
chr19:38787680..38788286hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625659
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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