A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370580



Internal ID21028133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97770085..97901781hg38UCSC Ensembl
chr3:97488929..97620625hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38131697
hg19131697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105538
Samples
Known GenesARL6, CRYBG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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