A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736357



Internal ID160023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29175230..29227823hg38UCSC Ensembl
chrX:29193347..29245940hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3852594
hg1952594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424708
Supporting Variants
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736357
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00270552


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