A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155445



Internal ID21462553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143818543..143818543hg38UCSC Ensembl
chr8:144900713..144900713hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642070
Supporting Variants
SamplesHG03009
Known GenesPUF60
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155445
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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