A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359990



Internal ID21017543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27644852..27647525hg38UCSC Ensembl
chr3:27686343..27689016hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg382674
hg192674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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