A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167775



Internal ID21404960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41211739..41211865hg38UCSC Ensembl
chrX:41070992..41071118hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671846
Supporting Variants
SamplesHG00512
Known GenesUSP9X
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167775
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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