A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355082



Internal ID21012635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165249621..165250211hg38UCSC Ensembl
chr2:166106131..166106721hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080637
Samples
Known GenesSCN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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