A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110316



Internal ID22019549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71255084..71255140hg38UCSC Ensembl
chrX:70474934..70474990hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648231
Samples
Known GenesBCYRN1, ZMYM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110316
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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