A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738199



Internal ID161865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155325606..155337606hg38UCSC Ensembl
chrX:154554922..154566915hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3812001
hg1911994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423970
Supporting Variants
Samples
Known GenesCLIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738199
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00210837


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