A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075855



Internal ID21415496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72278302..72278302hg38UCSC Ensembl
chr11:71989346..71989346hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382633
hg192633
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662557
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075855
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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