A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612237



Internal ID21560542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70840012..70840012hg38UCSC Ensembl
chr4:71705729..71705729hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124391, nssv17124361
SamplesHG03065, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612237
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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