A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646724



Internal ID21838771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71368911..71368977hg38UCSC Ensembl
chrX:70588761..70588827hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100567
Supporting Variants
Samples
Known GenesBCYRN1, TAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646724
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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