A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320816



Internal ID20853917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84502301..84510700hg38UCSC Ensembl
chr1:84967984..84976383hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205158
Samples
Known GenesGNG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320816
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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