A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166716



Internal ID21500384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27696695..27698075hg38UCSC Ensembl
chrX:27714812..27716192hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg381381
hg191381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668702
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166716
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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