A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547176



Internal ID20920381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57360028..57364243hg38UCSC Ensembl
chr20:55935084..55939299hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg384216
hg194216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203912
Samples
Known GenesMIR5095, RAE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547176
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer