A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109265



Internal ID22018498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29333447..29334209hg38UCSC Ensembl
chrX:29351564..29352326hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647649
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109265
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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