A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638470



Internal ID21586775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109579839..109579839hg38UCSC Ensembl
chr5:108915540..108915540hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134915
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638470
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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