A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738261



Internal ID161927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155902021..156003787hg38UCSC Ensembl
chrX:155131685..155233452hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38101767
hg19101768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424596
Supporting Variants
Samples
Known GenesIL9R, VAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738261
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00062461


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