A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045020



Internal ID20612060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17536910..17538146hg38UCSC Ensembl
chr19:17647719..17648955hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381237
hg191237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522150
Supporting Variants
Samples
Known GenesFAM129C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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