A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522169



Internal ID20895530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46186193..46281637hg38UCSC Ensembl
chr19:46689450..46784894hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3895445
hg1995445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198906
Samples
Known GenesDKFZp434J0226, IGFL1, RNU6-66P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522169
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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