A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340777



Internal ID20998330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28271569..28277640hg38UCSC Ensembl
chr2:28494436..28500507hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg386072
hg196072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087496
Samples
Known GenesBRE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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