A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648049



Internal ID21840096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103170278..103173112hg38UCSC Ensembl
chrX:102425206..102428040hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg382835
hg192835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648049
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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