A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112092



Internal ID22021326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40269702..40269760hg38UCSC Ensembl
chrX:40128955..40129013hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637563
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112092
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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