A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366696



Internal ID21024249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25697572..25936944hg38UCSC Ensembl
chr3:25739063..25978435hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38239373
hg19239373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101134
Samples
Known GenesLINC00692, NGLY1, OXSM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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