A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737298



Internal ID160964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118938017..118943331hg38UCSC Ensembl
chrX:118071980..118077294hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg385315
hg195315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420754
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737298
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00208117


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