A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928618



Internal ID22703860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57860066..57860231hg38UCSC Ensembl
chr17:55937427..55937592hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928618
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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