A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624425



Internal ID21572730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9940761..9940761hg38UCSC Ensembl
chr3:9982445..9982445hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138944
SamplesHG00513
Known GenesCRELD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624425
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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