A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100808



Internal ID22010041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105489707..105489825hg38UCSC Ensembl
chrX:104733699..104733817hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640904
Samples
Known GenesIL1RAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100808
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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