A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615285



Internal ID21563590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150969829..150969829hg38UCSC Ensembl
chrX:150138302..150138302hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381232
hg191232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166072
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615285
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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