A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579454



Internal ID21771497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63664773..63672747hg38UCSC Ensembl
chr10:65424533..65432507hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg387975
hg197975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001254
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579454
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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