A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941267



Internal ID22716689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83205505..83205912hg38UCSC Ensembl
chr17:81153274..81153681hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941267
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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