A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928779



Internal ID22704023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43217312..43217679hg38UCSC Ensembl
chr17:41369331..41369698hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384453
Samples
Known GenesTMEM106A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928779
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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