A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168545



Internal ID21482111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87697526..87760602hg38UCSC Ensembl
chrX:86952526..87015602hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3863077
hg1963077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668694
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168545
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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