A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614603



Internal ID21562908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4551595..4551595hg38UCSC Ensembl
chrX:4469636..4469636hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168007
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614603
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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