A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069687



Internal ID21512424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32164899..32165039hg38UCSC Ensembl
chr10:32453827..32453967hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585601
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069687
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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