A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933163



Internal ID22708472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69215768..69242040hg38UCSC Ensembl
chr17:67211909..67238181hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3826273
hg1926273
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383276
Samples
Known GenesABCA10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933163
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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