A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610647



Internal ID21558952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107401918..107401918hg38UCSC Ensembl
chrX:106645148..106645148hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164868
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610647
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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