A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345909



Internal ID21003462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183048570..183055816hg38UCSC Ensembl
chr2:183913298..183920544hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg387247
hg197247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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