A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355933



Internal ID21013486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24008326..24013199hg38UCSC Ensembl
chr4:24009949..24014822hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384874
hg194874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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