A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449260



Internal ID22507130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9895288..9895288hg38UCSC Ensembl
chr8:9752798..9752798hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449260
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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