A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205612



Internal ID20772652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159615001..159616700hg38UCSC Ensembl
chr2:160471512..160473211hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351445
Supporting Variants
Samples
Known GenesBAZ2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205612
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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