A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105884



Internal ID22015117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141950275..141950704hg38UCSC Ensembl
chrX:141038061..141038490hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105884
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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