A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619991



Internal ID20993062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158882541..158916042hg38UCSC Ensembl
chr6:159303573..159337074hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3833502
hg1933502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216711
Samples
Known GenesC6orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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