A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405135



Internal ID21062688
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 StatusM
Merged Variants
Supporting Variantsnssv18215034
Samples
Known GenesC5orf27, ELL2, GLRX, RHOBTB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405135
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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