A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637826



Internal ID21586131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102000595..102000595hg38UCSC Ensembl
chr10:103760352..103760352hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067465
SamplesHG00512
Known GenesC10orf76
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637826
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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