A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552989



Internal ID20926104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57326101..57335200hg38UCSC Ensembl
chr20:55901157..55910256hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203909
Samples
Known GenesSPO11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552989
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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