A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464487



Internal ID22522374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47086090..47089436hg38UCSC Ensembl
chrX:46945489..46948835hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg383347
hg193347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882241
Supporting Variants
Samples
Known GenesRGN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464487
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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