A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935066



Internal ID22710402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33202793..33208514hg38UCSC Ensembl
chr17:31529811..31535532hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg385722
hg195722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372286
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935066
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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