A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067636



Internal ID21479015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125405047..125405109hg38UCSC Ensembl
chr10:127093616..127093678hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590006
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067636
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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