A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533733



Internal ID20907094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11491645..11515651hg38UCSC Ensembl
chr19:11602460..11626466hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3824007
hg1924007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045009
Samples
Known GenesECSIT, MIR7974, ZNF653
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533733
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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