A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533352



Internal ID20906713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44585589..44621254hg38UCSC Ensembl
chr19:45088848..45124552hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3835666
hg1935705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198845
Samples
Known GenesIGSF23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533352
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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