A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668796



Internal ID21617101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71452079..71452131hg38UCSC Ensembl
chrX:70671929..70671981hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167736
SamplesNA20847
Known GenesBCYRN1, TAF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668796
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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