A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168546



Internal ID21479480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87716968..87717073hg38UCSC Ensembl
chrX:86971968..86972073hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671545
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168546
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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