A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522317



Internal ID20895678
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 StatusM
Merged Variants
Supporting Variantsnssv18047215
Samples
Known GenesOR7C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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