A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618621



Internal ID21810668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58863530..58863530hg38UCSC Ensembl
chr18:56530762..56530762hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110651
Supporting Variants
Samples
Known GenesZNF532
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618621
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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