A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053344



Internal ID21962577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5288811..5288811hg38UCSC Ensembl
chrX:5206852..5206852hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053344
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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