A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348094



Internal ID21005647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:49432363..49517026hg38UCSC Ensembl
chr2:49659501..49744164hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3884664
hg1984664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3859n223
Supporting Variantsnssv18086124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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