A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350679



Internal ID21008232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36553425..36555977hg38UCSC Ensembl
chr2:36780568..36783120hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg382553
hg192553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089046
Samples
Known GenesFEZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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