A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067468



Internal ID21511895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102087102..102092459hg38UCSC Ensembl
chr10:103846859..103852216hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385358
hg195358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600032
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067468
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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