A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928191



Internal ID22703427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75302749..75312507hg38UCSC Ensembl
chr17:73298830..73308588hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg389759
hg199759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928191
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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