A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146426



Internal ID21472402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81142503..81142503hg38UCSC Ensembl
chr8:82054738..82054738hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631502
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146426
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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