A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626603



Internal ID21574908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62947532..62947532hg38UCSC Ensembl
chr10:64707292..64707292hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070460
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626603
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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