A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046638



Internal ID21955871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45334530..45334530hg38UCSC Ensembl
chrX:45193775..45193775hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046638
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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