A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425906



Internal ID22483776
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 StatusS
Merged Variantsnsv5892169
Supporting Variants
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425906
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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