A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516372



Internal ID20889733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2510321..2519032hg38UCSC Ensembl
chr19:2510319..2519030hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388712
hg198712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046036
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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