A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619169



Internal ID21567474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38854890..38854890hg38UCSC Ensembl
chrX:38714143..38714143hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167366
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619169
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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