A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641992



Internal ID21834039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71339903..71339970hg38UCSC Ensembl
chrX:70559753..70559820hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103406
Supporting Variants
Samples
Known GenesBCYRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641992
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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