A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110922



Internal ID22020155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2999526..3003479hg38UCSC Ensembl
chrX:2917567..2921520hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg383954
hg193954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110922
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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