A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371369



Internal ID21028922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22623440..22625745hg38UCSC Ensembl
chr4:22625063..22627368hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382306
hg192306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371369
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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