A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103868



Internal ID22013101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64009214..64024279hg38UCSC Ensembl
chrX:63229094..63244159hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3815066
hg1915066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103868
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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