A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737180



Internal ID160846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105144400..105150171hg38UCSC Ensembl
chrX:104389083..104394854hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg385772
hg195772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138002
Supporting Variants
Samples
Known GenesIL1RAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737180
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00397573


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