A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075799



Internal ID21415475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69715077..69715077hg38UCSC Ensembl
chr11:69529845..69529845hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653427
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075799
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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