A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623433



Internal ID21571738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35621837..35621837hg38UCSC Ensembl
chrX:35639954..35639954hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166829
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623433
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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