A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110832



Internal ID22020065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:143801643..143801719hg38UCSC Ensembl
chrX:142884738..142884814hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110832
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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