A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738264



Internal ID161930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155965606..156029606hg38UCSC Ensembl
chrX:155195271..155259271hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3864001
hg1964001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138548
Supporting Variants
Samples
Known GenesIL9R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738264
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000209468


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