A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631779



Internal ID21823826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35306020..35306141hg38UCSC Ensembl
chr19:35796923..35797044hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047441
Supporting Variants
Samples
Known GenesMAG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631779
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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