A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101645



Internal ID22010879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:126311087..126331535hg38UCSC Ensembl
chrX:125445070..125465518hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3820449
hg1920449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101645
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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