A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111462



Internal ID22020696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15783951..15784018hg38UCSC Ensembl
chrX:15802074..15802141hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637984
Samples
Known GenesCA5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111462
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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