A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522404



Internal ID20895765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16012601..16021700hg38UCSC Ensembl
chr19:16123411..16132510hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044458
Samples
Known GenesLINC00661
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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