A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364550



Internal ID21022103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32885731..32913957hg38UCSC Ensembl
chr4:32887353..32915579hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3828227
hg1928227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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