A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111397



Internal ID22020631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80473538..80547809hg38UCSC Ensembl
chrX:79729037..79803308hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3874272
hg1974272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111397
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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