A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048821



Internal ID21958056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1514420..1514420hg38UCSC Ensembl
chrX:1633313..1633313hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648067
Samples
Known GenesP2RY8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048821
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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