A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634976



Internal ID21583281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50659361..50659361hg38UCSC Ensembl
chr10:52419121..52419121hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070315
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634976
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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