A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111163



Internal ID22020396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71506501..71507261hg38UCSC Ensembl
chrX:70726351..70727111hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641836
Samples
Known GenesBCYRN1, TAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111163
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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