A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466236



Internal ID22524126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9730207..9730376hg38UCSC Ensembl
chrX:9698247..9698416hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887204
Supporting Variants
Samples
Known GenesGPR143
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466236
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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