A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372484



Internal ID21030037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22244718..22245272hg38UCSC Ensembl
chr4:22246341..22246895hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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