A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167737



Internal ID21450263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71520430..71522095hg38UCSC Ensembl
chrX:70740280..70741945hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg381666
hg191666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670097
Supporting Variants
SamplesHG01114
Known GenesBCYRN1, TAF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167737
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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