A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053751



Internal ID21962984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94762571..94762571hg38UCSC Ensembl
chrX:94017570..94017570hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053751
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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