A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167596



Internal ID21446447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47233763..47233815hg38UCSC Ensembl
chrX:47093162..47093214hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668460
Supporting Variants
SamplesHG00732
Known GenesUSP11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167596
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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