A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060446



Internal ID21969680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40530441..40530441hg38UCSC Ensembl
chrX:40389693..40389693hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060446
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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