A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899875



Internal ID22675011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113254198..113256578hg38UCSC Ensembl
chr6:113575400..113577780hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382381
hg192381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899875
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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