A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060015



Internal ID21969249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46219470..46219470hg38UCSC Ensembl
chrX:46078905..46078905hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060015
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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