A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617733



Internal ID21566038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46317126..46317126hg38UCSC Ensembl
chrX:46176561..46176561hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167566
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617733
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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