A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105035



Internal ID22014268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29374976..29377399hg38UCSC Ensembl
chrX:29393093..29395516hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg382424
hg192424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640486
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105035
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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