A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252401



Internal ID22057011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29475765..29475765hg38UCSC Ensembl
chrX:29493882..29493882hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851840
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252401
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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