A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168972



Internal ID21475355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92928276..92928474hg38UCSC Ensembl
chrX:92183275..92183473hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666955
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168972
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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