A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057476



Internal ID21966709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112954482..112954482hg38UCSC Ensembl
chrX:112197710..112197710hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057476
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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