A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101446



Internal ID22010679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155691851..155692063hg38UCSC Ensembl
chrX:154921512..154921724hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101446
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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