A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940880



Internal ID22716294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64218500..64227775hg38UCSC Ensembl
chr17:62295860..62305135hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg389276
hg199276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379052
Samples
Known GenesTEX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940880
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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