A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074172



Internal ID21451336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29489321..29489321hg38UCSC Ensembl
chr11:29510868..29510868hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660971
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074172
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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