A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072929



Internal ID21406605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122836537..122836537hg38UCSC Ensembl
chr11:122707245..122707245hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656712
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072929
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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