A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530778



Internal ID20904139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14470115..14472302hg38UCSC Ensembl
chr19:14580927..14583114hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382188
hg192188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045940
Samples
Known GenesPKN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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