A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525596



Internal ID20898957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:760727..930692hg38UCSC Ensembl
chr20:741371..911335hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38169966
hg19169965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4351n223
Supporting Variantsnssv18204084
Samples
Known GenesANGPT4, FAM110A, SLC52A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525596
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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