A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417737



Internal ID21075290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55808595..55967439hg38UCSC Ensembl
chr8:56721154..56879998hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38158845
hg19158845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219694
Samples
Known GenesLYN, TGS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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