A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074868



Internal ID21438327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61377729..61377729hg38UCSC Ensembl
chr11:61145201..61145201hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653793
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074868
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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