A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167278



Internal ID21500488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43809946..43810267hg38UCSC Ensembl
chrX:43669193..43669514hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670926
Supporting Variants
SamplesNA19239
Known GenesMAOB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167278
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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