A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066693



Internal ID21511319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111242688..111242754hg38UCSC Ensembl
chr10:113002446..113002512hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595354
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066693
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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