A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068120



Internal ID21510438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23134569..23134569hg38UCSC Ensembl
chr10:23423498..23423498hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640759
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068120
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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