A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112427



Internal ID22021660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44609807..44609877hg38UCSC Ensembl
chrX:44469053..44469123hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112427
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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