A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068311



Internal ID21435503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110411738..110411738hg38UCSC Ensembl
chr10:112171496..112171496hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630560
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068311
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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