A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631725



Internal ID21823772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56377660..56377660hg38UCSC Ensembl
chr19:56889029..56889029hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111566
Supporting Variants
Samples
Known GenesZNF542
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631725
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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