A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625661



Internal ID21817708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32246793..32247091hg38UCSC Ensembl
chr18:29826756..29827054hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625661
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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