A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521559



Internal ID20894920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19075404..19080522hg38UCSC Ensembl
chr19:19186213..19191331hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg385119
hg195119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045970
Samples
Known GenesSLC25A42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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