A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168437



Internal ID21492401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79864707..79864783hg38UCSC Ensembl
chrX:79120207..79120283hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666830
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168437
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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