A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069499



Internal ID21466537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16295032..16295091hg38UCSC Ensembl
chr10:16337031..16337090hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589449
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069499
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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