A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076896



Internal ID21403085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9864387..9864387hg38UCSC Ensembl
chr11:9885934..9885934hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648535
Supporting Variants
SamplesHG00171
Known GenesSBF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076896
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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