A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928036



Internal ID22703271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72320354..72320410hg38UCSC Ensembl
chr17:70316495..70316551hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928036
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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