A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445084



Internal ID22502954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42182378..42182378hg38UCSC Ensembl
chr8:42039896..42039896hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951842
Supporting Variants
Samples
Known GenesPLAT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445084
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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