A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412471



Internal ID21070024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53669550..53670134hg38UCSC Ensembl
chr5:52965380..52965964hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132386
Samples
Known GenesNDUFS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412471
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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