A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589416



Internal ID21781459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63146132..63146132hg38UCSC Ensembl
chr10:64905892..64905892hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088712
Supporting Variants
Samples
Known GenesNRBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589416
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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