A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366199



Internal ID21023752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32881282..32883308hg38UCSC Ensembl
chr4:32882904..32884930hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382027
hg192027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115586
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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