A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344499



Internal ID21002052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:30277835..30300120hg38UCSC Ensembl
chr2:30500701..30522986hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3822286
hg1922286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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