A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530659



Internal ID20904020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:903936..911325hg38UCSC Ensembl
chr19:903936..911325hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387390
hg197390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050097
Samples
Known GenesR3HDM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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