A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104152



Internal ID22013387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29382063..29382580hg38UCSC Ensembl
chrX:29400180..29400697hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642727
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104152
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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