A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449259



Internal ID21106812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96162101..96164200hg38UCSC Ensembl
chr10:97921857..97923956hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985326
Samples
Known GenesZNF518A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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