A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532021



Internal ID20905382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57497316..57510836hg38UCSC Ensembl
chr19:58008684..58022204hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3813521
hg1913521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199709
Samples
Known GenesZNF773
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532021
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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