A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452573



Internal ID21110126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132134111..132138214hg38UCSC Ensembl
chr10:133947615..133951718hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg384104
hg194104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978530
Samples
Known GenesJAKMIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452573
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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