A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618779



Internal ID21810826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36195535..36195831hg38UCSC Ensembl
chr19:36686437..36686733hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047086
Supporting Variants
Samples
Known GenesZNF565
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618779
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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