A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892169



Internal ID22667215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110335475..110335582hg38UCSC Ensembl
chr6:110656678..110656785hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425906
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892169
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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