A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902909



Internal ID22678071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95560758..95564062hg38UCSC Ensembl
chr5:94896462..94899766hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383305
hg193305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419865
Samples
Known GenesARSK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902909
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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