A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362811



Internal ID21020364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102027001..102028900hg38UCSC Ensembl
chr3:101745845..101747744hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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