A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048059



Internal ID20615099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4114900..4116430hg38UCSC Ensembl
chr19:4114898..4116428hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381531
hg191531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531995
Supporting Variants
Samples
Known GenesMAP2K2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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