A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075475



Internal ID21483905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68207790..68207790hg38UCSC Ensembl
chr11:67975257..67975257hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663657
Supporting Variants
SamplesNA12329
Known GenesSUV420H1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075475
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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