A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634163



Internal ID21582468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17172042..17172042hg38UCSC Ensembl
chr5:17172151..17172151hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg381687
hg191687
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122859
SamplesNA19239
Known GenesLOC285696
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634163
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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