A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626792



Internal ID21575097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92638242..92638242hg38UCSC Ensembl
chr5:91973949..91973949hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151918
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626792
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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