A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551427



Internal ID20924561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49869638..49902999hg38UCSC Ensembl
chr20:48486175..48519536hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3833362
hg1933362
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202985
Samples
Known GenesSLC9A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551427
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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