A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043286



Internal ID21952592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75232710..75232710hg38UCSC Ensembl
chrX:74452545..74452545hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043286
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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