A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453326



Internal ID21110879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24752088..24766293hg38UCSC Ensembl
chr10:25041017..25055222hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3814206
hg1914206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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