A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932593



Internal ID22707894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62451490..62452375hg38UCSC Ensembl
chr17:60528851..60529736hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932593
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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