A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049939



Internal ID20616979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5905104..5908239hg38UCSC Ensembl
chr19:5905115..5908250hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383136
hg193136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529759
Supporting Variants
Samples
Known GenesVMAC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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