A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667898



Internal ID21616204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:83354773..83354822hg38UCSC Ensembl
chrX:82609781..82609830hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168674
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667898
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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