A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108995



Internal ID22018228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40110667..40110722hg38UCSC Ensembl
chrX:39969920..39969975hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649801
Samples
Known GenesBCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108995
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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