A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618340



Internal ID21566645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158228874..158228874hg38UCSC Ensembl
chr3:157946663..157946663hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120993, nssv17137701
SamplesHG00731, HG00732
Known GenesRSRC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618340
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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