A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517966



Internal ID20891327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31594163..31637367hg38UCSC Ensembl
chr20:30181966..30225170hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3843205
hg1943205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202658
Samples
Known GenesID1, MIR3193
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517966
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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