A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737511



Internal ID161177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123972320..123973986hg38UCSC Ensembl
chrX:123106170..123107836hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381667
hg191667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425298
Supporting Variants
Samples
Known GenesSTAG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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