A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894566



Internal ID22669639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107283682..107283987hg38UCSC Ensembl
chr6:107604886..107605191hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415462
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894566
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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