A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637875



Internal ID21586180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77971906..77971906hg38UCSC Ensembl
chr10:79731664..79731664hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071446
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637875
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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