A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375455



Internal ID21033008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32341698..32342038hg38UCSC Ensembl
chr3:32383190..32383530hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099388
Samples
Known GenesCMTM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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