A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338489



Internal ID20996042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11417691..11419452hg38UCSC Ensembl
chr2:11557817..11559578hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381762
hg191762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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