A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135606



Internal ID20702647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95560864..95563972hg38UCSC Ensembl
chr5:94896568..94899676hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383109
hg193109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397735
Supporting Variants
Samples
Known GenesARSK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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