A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402134



Internal ID21059687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53580976..53584880hg38UCSC Ensembl
chr5:52876806..52880710hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg383905
hg193905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132376
Samples
Known GenesNDUFS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402134
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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