A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388145



Internal ID21045698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:23517110..23517744hg38UCSC Ensembl
chr5:23517219..23517853hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129385
Samples
Known GenesPRDM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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