A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612785



Internal ID21561090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52632918..52632918hg38UCSC Ensembl
chr4:53499085..53499085hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138190
SamplesNA18939
Known GenesUSP46
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612785
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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