A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108972



Internal ID22018205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73907667..73915383hg38UCSC Ensembl
chrX:73127502..73135218hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg387717
hg197717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108972
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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