A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372598



Internal ID21030151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3079065..3088299hg38UCSC Ensembl
chr3:3120749..3129983hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg389235
hg199235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099300
Samples
Known GenesIL5RA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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