A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523893



Internal ID20897254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52330003..52345884hg38UCSC Ensembl
chr19:52833256..52849137hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3815882
hg1915882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198330
Samples
Known GenesZNF610
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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