A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148149



Internal ID21467964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8617402..8617402hg38UCSC Ensembl
chr8:8474912..8474912hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640608
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148149
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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