A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737017



Internal ID160683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53070563..53070975hg38UCSC Ensembl
chrX:53099745..53100157hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417490
Supporting Variants
Samples
Known GenesGPR173
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737017
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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