A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156492



Internal ID21479268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91545757..91545757hg38UCSC Ensembl
chr8:92557985..92557985hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633819
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156492
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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