A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668694



Internal ID21616999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87697526..87760602hg38UCSC Ensembl
chrX:86952526..87015602hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3863077
hg1963077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168545
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668694
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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