A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670488



Internal ID21618793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132805403..132807513hg38UCSC Ensembl
chrX:131939431..131941541hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg382111
hg192111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165697
SamplesHG02492
Known GenesHS6ST2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670488
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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