A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533982



Internal ID20907343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11588601..11623000hg38UCSC Ensembl
chr19:11699416..11733815hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3834400
hg1934400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045016
Samples
Known GenesZNF627
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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