A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080637



Internal ID20647677
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 StatusS
Merged Variantsnsv6355082
Supporting Variants
Samples
Known GenesSCN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


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