A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166086



Internal ID21511879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1514422..1514542hg38UCSC Ensembl
chrX:1633315..1633435hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668405
Supporting Variants
SamplesNA24385
Known GenesP2RY8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166086
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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