A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359979



Internal ID21017532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32461327..32466773hg38UCSC Ensembl
chr3:32502819..32508265hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385447
hg195447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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