A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215034



Internal ID20782074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95768680..95951039hg38UCSC Ensembl
chr5:95104384..95286743hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38182360
hg19182360
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405135
Supporting Variants
Samples
Known GenesC5orf27, ELL2, GLRX, RHOBTB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215034
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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