A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625990



Internal ID21818037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49080016..49080114hg38UCSC Ensembl
chr18:46606386..46606484hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023091
Supporting Variants
Samples
Known GenesDYM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625990
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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