A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523628



Internal ID20896989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36928626..36932293hg38UCSC Ensembl
chr20:35557029..35560696hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg383668
hg193668
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202224
Samples
Known GenesSAMHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523628
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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