A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737412



Internal ID161078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121546376..121548363hg38UCSC Ensembl
chrX:120680230..120682217hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg381988
hg191988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737412
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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