A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106592



Internal ID22015826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69421915..69422072hg38UCSC Ensembl
chrX:68641758..68641915hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640146
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106592
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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