A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620995



Internal ID21813042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30037006..30038175hg38UCSC Ensembl
chr19:30527913..30529082hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620995
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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