A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666093



Internal ID21614398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71703190..71749804hg38UCSC Ensembl
chrX:70923040..70969654hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3846615
hg1946615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167743
SamplesNA19983
Known GenesBCYRN1, CXorf49, CXorf49B, LINC00891, LOC100132741
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666093
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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