A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054013



Internal ID21963246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11760172..11760172hg38UCSC Ensembl
chrX:11778291..11778291hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644068
Samples
Known GenesMSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054013
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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