A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529338



Internal ID20902699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12040367..12050966hg38UCSC Ensembl
chr19:12151182..12161781hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3442n223
Supporting Variantsnssv18044905
Samples
Known GenesZNF878
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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