A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519952



Internal ID20893313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7364501..7377700hg38UCSC Ensembl
chr20:7345148..7358347hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3813200
hg1913200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070610
Samples
Known GenesMIR8062
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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