A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076268



Internal ID21440229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82946809..82946809hg38UCSC Ensembl
chr11:82657851..82657851hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651650
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076268
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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