A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646092



Internal ID21838139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119286378..119340544hg38UCSC Ensembl
chrX:118420341..118474507hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3854167
hg1954167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646092
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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