A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443576



Internal ID22501446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155999763..156029758hg38UCSC Ensembl
chrX:155229428..155259423hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3829996
hg1929996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881556
Supporting Variants
Samples
Known GenesIL9R
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443576
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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