A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379933



Internal ID21037486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24748763..24762400hg38UCSC Ensembl
chr5:24748872..24762509hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3813638
hg1913638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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