A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339488



Internal ID20997041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2486230..2491183hg38UCSC Ensembl
chr2:2490002..2494955hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg384954
hg194954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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