A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049051



Internal ID21958284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101098980..101098980hg38UCSC Ensembl
chrX:100353969..100353969hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049051
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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