A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441346



Internal ID22499216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42309814..42310130hg38UCSC Ensembl
chr6:42277552..42277868hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898386
Supporting Variants
Samples
Known GenesTRERF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441346
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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