A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941620



Internal ID22717047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81690486..81690552hg38UCSC Ensembl
chr17:79657516..79657582hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377574
Samples
Known GenesHGS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941620
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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