A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604079



Internal ID21552746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6413682..6413732hg38UCSC Ensembl
chr10:6455644..6455694hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071223
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604079
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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