A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897192



Internal ID22672291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121640297..121649753hg38UCSC Ensembl
chr6:121961443..121970899hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg389457
hg199457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897192
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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