A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646960



Internal ID21839007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116011016..116011080hg38UCSC Ensembl
chrX:115127349..115127413hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646960
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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