A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636398



Internal ID21584703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59694817..59694817hg38UCSC Ensembl
chr10:61454575..61454575hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071174
SamplesNA19650
Known GenesSLC16A9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636398
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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