A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023616



Internal ID21932959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74503792..74503951hg38UCSC Ensembl
chr18:72171027..72171186hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630056
Samples
Known GenesCNDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023616
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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