A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532250



Internal ID20905611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10576576..10577614hg38UCSC Ensembl
chr19:10687252..10688290hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198035
Samples
Known GenesAP1M2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532250
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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