A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522144



Internal ID20895505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4204980..4205885hg38UCSC Ensembl
chr19:4204977..4205882hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197428
Samples
Known GenesANKRD24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522144
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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