A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639466



Internal ID21587771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107462602..107462602hg38UCSC Ensembl
chr5:106798303..106798303hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126126
SamplesHG03371
Known GenesEFNA5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639466
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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