A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167808



Internal ID21404856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42653036..42654617hg38UCSC Ensembl
chrX:42512288..42513869hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665893
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167808
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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