A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050491



Internal ID21959724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38925747..38925747hg38UCSC Ensembl
chrX:38785001..38785001hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050491
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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