A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098236



Internal ID21401680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:116853..116853hg38UCSC Ensembl
chr11:179813..179813hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg385451
hg195451
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660405
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098236
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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