A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359536



Internal ID21017089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97834970..97835613hg38UCSC Ensembl
chr3:97553814..97554457hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105545
Samples
Known GenesCRYBG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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