A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167248



Internal ID21475958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3383132..3383370hg38UCSC Ensembl
chrX:3301173..3301411hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668286
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167248
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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