A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047215



Internal ID20614255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14937235..14942741hg38UCSC Ensembl
chr19:15048047..15053553hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385507
hg195507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522317
Supporting Variants
Samples
Known GenesOR7C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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