A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203784



Internal ID22352740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71358970..71359543hg38UCSC Ensembl
chrX:70578820..70579393hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352171
SamplesNA19239
Known GenesBCYRN1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203784
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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