A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365090



Internal ID21022643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183557389..183559264hg38UCSC Ensembl
chr3:183275177..183277052hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381876
hg191876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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