A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263019



Internal ID20472237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18609226..18622755hg38UCSC Ensembl
chr10:18898155..18911684hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3813530
hg1913530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744042
Supporting Variants
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263019
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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