A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610695



Internal ID21559000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26831704..26831704hg38UCSC Ensembl
chrX:26849821..26849821hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166604
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610695
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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