A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453425



Internal ID21110978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109165093..109287196hg38UCSC Ensembl
chr10:110924851..111046954hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38122104
hg19122104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979443
Samples
Known GenesRNU6-53P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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