A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372685



Internal ID21030238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36549464..36551885hg38UCSC Ensembl
chr3:36590956..36593377hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382422
hg192422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372685
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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