A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637022



Internal ID21829069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2939072..2939072hg38UCSC Ensembl
chr19:2939070..2939070hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106658
Supporting Variants
Samples
Known GenesZNF77
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637022
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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