A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358638



Internal ID21016191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146917996..146919560hg38UCSC Ensembl
chr3:146635783..146637347hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096238
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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