A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368544



Internal ID21026097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97839481..97839993hg38UCSC Ensembl
chr3:97558325..97558837hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105546
Samples
Known GenesCRYBG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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