A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056872



Internal ID21966107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29394523..29394523hg38UCSC Ensembl
chrX:29412640..29412640hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639638
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056872
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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