A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103688



Internal ID22012921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77930222..77932439hg38UCSC Ensembl
chrX:77185719..77187936hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg382218
hg192218
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644345
Samples
Known GenesATP7A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103688
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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