A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057600



Internal ID21966833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31031396..31031396hg38UCSC Ensembl
chrX:31049513..31049513hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647859
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057600
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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