A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519145



Internal ID20892506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14071651..14280291hg38UCSC Ensembl
chr18:14071650..14280290hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38208641
hg19208641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039254
Samples
Known GenesANKRD20A5P, ZNF519
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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