A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541595



Internal ID20914877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31836979..31839264hg38UCSC Ensembl
chr22:32232965..32235250hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382286
hg192286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073752
Samples
Known GenesDEPDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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