A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614092



Internal ID21562397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37036684..37036684hg38UCSC Ensembl
chr4:37038306..37038306hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128824, nssv17119948
SamplesHG03486, HG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614092
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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