A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940494



Internal ID22715903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68821767..68826161hg38UCSC Ensembl
chr17:66817908..66822302hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg384395
hg194395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940494
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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