A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599970



Internal ID21548608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10767840..10768009hg38UCSC Ensembl
chr10:10809803..10809972hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067490
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599970
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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