A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628441



Internal ID21820488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29566135..29566217hg38UCSC Ensembl
chr19:30057042..30057124hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628441
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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