A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352950



Internal ID21010503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5554955..5557786hg38UCSC Ensembl
chr2:5695087..5697918hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg382832
hg192832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352950
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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