A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640334



Internal ID21832381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71452109..71452164hg38UCSC Ensembl
chrX:70671959..70672014hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103936
Supporting Variants
Samples
Known GenesBCYRN1, TAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640334
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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