A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615766



Internal ID21564071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78178947..78178947hg38UCSC Ensembl
chrX:77434444..77434444hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168185
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615766
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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