A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054513



Internal ID21963746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21731500..21731500hg38UCSC Ensembl
chrX:21749618..21749618hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646460
Samples
Known GenesSMPX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054513
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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