A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068700



Internal ID21487966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124792666..124792666hg38UCSC Ensembl
chr10:126481235..126481235hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643876
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068700
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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