A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737286



Internal ID160952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118796841..118796932hg38UCSC Ensembl
chrX:117930804..117930895hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431781
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737286
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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