A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647219



Internal ID21839266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71341285..71341416hg38UCSC Ensembl
chrX:70561135..70561266hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104033
Supporting Variants
Samples
Known GenesBCYRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647219
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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