A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638848



Internal ID21830895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45746857..45746912hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638848
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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