A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107639



Internal ID22016872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147279105..147287194hg38UCSC Ensembl
chrX:146360623..146368712hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg388090
hg198090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648187
Samples
Known GenesMIR514A1, MIR514A2, MIR514A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107639
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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