A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963548



Internal ID22738483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32739555..32740226hg38UCSC Ensembl
chr20:31327362..31328033hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406452
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963548
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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