A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370252



Internal ID21027805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142435304..142435966hg38UCSC Ensembl
chr3:142154146..142154808hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094347
Samples
Known GenesXRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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