A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071146



Internal ID21499885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6925997..6925997hg38UCSC Ensembl
chr10:6967959..6967959hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635245
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071146
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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