A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363157



Internal ID21020710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6096774..6129732hg38UCSC Ensembl
chr3:6138461..6171419hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3832959
hg1932959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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