A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737869



Internal ID161535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148105488..148105690hg38UCSC Ensembl
chrX:147187008..147187210hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414664
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737869
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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