A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075716



Internal ID21457805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77706997..77706997hg38UCSC Ensembl
chr11:77418042..77418042hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648076
Supporting Variants
SamplesHG02587
Known GenesRSF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075716
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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