A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437546



Internal ID21095099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98275348..98279522hg38UCSC Ensembl
chr10:100035105..100039279hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg384175
hg194175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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