A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531363



Internal ID20904724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12388193..12427739hg38UCSC Ensembl
chr19:12499007..12538553hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839547
hg1939547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3443n223
Supporting Variantsnssv18197343
Samples
Known GenesZNF799
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531363
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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