A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338286



Internal ID20995839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:146566001..146567800hg38UCSC Ensembl
chr2:147323569..147325368hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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