A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357166



Internal ID21014719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108322394..108323140hg38UCSC Ensembl
chr3:108041241..108041987hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093304
Samples
Known GenesHHLA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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