A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368939



Internal ID21026492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:80495373..80607702hg38UCSC Ensembl
chr3:80544523..80656853hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38112330
hg19112331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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