A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936722



Internal ID22712080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68566974..68569153hg38UCSC Ensembl
chr17:66563115..66565294hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg382180
hg192180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv924n209
Supporting Variantsnssv17377493
Samples
Known GenesFAM20A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936722
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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