A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988710



Internal ID20555750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19398151..19400291hg38UCSC Ensembl
chr11:19419698..19421838hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382141
hg192141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449003
Supporting Variants
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988710
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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