A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529177



Internal ID20902538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17527601..17535500hg38UCSC Ensembl
chr20:17508246..17516145hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4421n223
Supporting Variantsnssv18205239
Samples
Known GenesBFSP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529177
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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