A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352793



Internal ID21010346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28276531..28277174hg38UCSC Ensembl
chr2:28499398..28500041hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087497
Samples
Known GenesBRE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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