A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167575



Internal ID21445077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46497285..46497450hg38UCSC Ensembl
chrX:46356720..46356885hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671604
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167575
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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