A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402042



Internal ID21059595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53565979..53585526hg38UCSC Ensembl
chr5:52861809..52881356hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3819548
hg1919548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132374
Samples
Known GenesNDUFS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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