A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524027



Internal ID20897388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19708601..19730200hg38UCSC Ensembl
chr19:19819410..19841009hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3821600
hg1921600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198381
Samples
Known GenesZNF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524027
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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