A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540196



Internal ID20913488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62575092..62784363hg38UCSC Ensembl
chr20:61172299..61415715hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38209272
hg19243417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203415
Samples
Known GenesLINC00659, LOC100127888, NTSR1, SLCO4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540196
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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