A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737340



Internal ID161006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119760894..119767925hg38UCSC Ensembl
chrX:118894857..118901888hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg387032
hg197032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429038
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737340
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0118701


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