A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463038



Internal ID22520923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40080079..40080158hg38UCSC Ensembl
chrX:39939332..39939411hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869940
Supporting Variants
Samples
Known GenesBCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463038
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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