A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370793



Internal ID21028346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182006963..182007926hg38UCSC Ensembl
chr3:181724751..181725714hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097825
Samples
Known GenesLOC100996490
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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