A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109874



Internal ID22019107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43192285..43414225hg38UCSC Ensembl
chrX:43051534..43273474hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38221941
hg19221941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109874
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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