A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516877



Internal ID20890238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32387411..32388279hg38UCSC Ensembl
chr19:32878317..32879185hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38869
hg19869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197309
Samples
Known GenesZNF507
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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