A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410039



Internal ID21067592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96231356..96327822hg38UCSC Ensembl
chr5:95567060..95663526hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3896467
hg1996467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135651
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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