A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533203



Internal ID20906564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12960119..12973033hg38UCSC Ensembl
chr19:13070933..13083847hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812915
hg1912915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045386
Samples
Known GenesDAND5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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