A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387520



Internal ID21045073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12235191..12308057hg38UCSC Ensembl
chr5:12235303..12308169hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3872867
hg1972867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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