A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409408



Internal ID21066961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110762496..110763336hg38UCSC Ensembl
chr5:110098196..110099036hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124922
Samples
Known GenesSLC25A46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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