A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897081



Internal ID22672179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23159526..23161336hg38UCSC Ensembl
chr6:23159754..23161564hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381811
hg191811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897081
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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