A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535262



Internal ID20908623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12912028..12912442hg38UCSC Ensembl
chr19:13022842..13023256hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045384
Samples
Known GenesSYCE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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