A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354076



Internal ID21011629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170964433..170989755hg38UCSC Ensembl
chr2:171820943..171846265hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3825323
hg1925323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207398
Samples
Known GenesGORASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354076
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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