A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800579



Internal ID21245917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108689609..108689609hg38UCSC Ensembl
chr1:109232231..109232231hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680778, nssv13677028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800579
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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