A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076169



Internal ID21415633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76619300..76619300hg38UCSC Ensembl
chr11:76330344..76330344hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662266
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076169
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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