A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612975



Internal ID21561280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21424301..21424301hg38UCSC Ensembl
chr3:21465793..21465793hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122135, nssv17121561
SamplesHG00731, HG00732
Known GenesZNF385D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612975
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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