A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429022



Internal ID207880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29581981..29590923hg38UCSC Ensembl
chrX:29600098..29609040hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg388943
hg198943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736371
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429022
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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