A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410251



Internal ID21067804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122986293..122991461hg38UCSC Ensembl
chr5:122321988..122327156hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg385169
hg195169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123858
Samples
Known GenesSNX24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410251
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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