A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617869



Internal ID21809916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30384138..30384138hg38UCSC Ensembl
chr19:30875045..30875045hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108601
Supporting Variants
Samples
Known GenesZNF536
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617869
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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