A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620767



Internal ID21569072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37653417..37653417hg38UCSC Ensembl
chr4:37655039..37655039hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125059
SamplesNA19238
Known GenesRELL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620767
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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