A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041755



Internal ID21951085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25042010..25042010hg38UCSC Ensembl
chrX:25060127..25060127hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041755
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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