A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046688



Internal ID20613728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3788776..3789965hg38UCSC Ensembl
chr19:3788774..3789963hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516070
Supporting Variants
Samples
Known GenesMATK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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