A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370813



Internal ID21028366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130754008..130756154hg38UCSC Ensembl
chr3:130472852..130474998hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382147
hg192147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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