A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618150



Internal ID21566455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90165497..90165497hg38UCSC Ensembl
chrX:89420496..89420496hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168586
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618150
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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