A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052908



Internal ID21962141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71557787..71557787hg38UCSC Ensembl
chrX:70777637..70777637hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641423
Samples
Known GenesBCYRN1, OGT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052908
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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