A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519351



Internal ID20892712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20119147..20197745hg38UCSC Ensembl
chr19:20229956..20308554hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3878599
hg1978599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045486
Samples
Known GenesZNF486, ZNF90
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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