A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041995



Internal ID21951320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32739566..32740231hg38UCSC Ensembl
chr20:31327373..31328038hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626741
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041995
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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