A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523307



Internal ID20896668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16711449..16723904hg38UCSC Ensembl
chr19:16822260..16834715hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3812456
hg1912456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197677
Samples
Known GenesNWD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523307
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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