A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109287



Internal ID22018520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41380247..41510400hg38UCSC Ensembl
chrX:41239500..41369653hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38130154
hg19130154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649576
Samples
Known GenesNYX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109287
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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