A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112130



Internal ID22021364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95857926..96199150hg38UCSC Ensembl
chrX:95112925..95454149hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38341225
hg19341225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112130
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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