A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737294



Internal ID160960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118897566..118916000hg38UCSC Ensembl
chrX:118031529..118049963hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3818435
hg1918435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6137954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737294
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000627484


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