A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527635



Internal ID20900996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45627106..45629471hg38UCSC Ensembl
chr19:46130364..46132729hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382366
hg192366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046516
Samples
Known GenesEML2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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