A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372619



Internal ID21030172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58398221..58401434hg38UCSC Ensembl
chr3:58383948..58387161hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg383214
hg193214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102940
Samples
Known GenesPXK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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