A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502109



Internal ID20875350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58660670..58682701hg38UCSC Ensembl
chr16:58694574..58716605hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3822032
hg1922032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030875
Samples
Known GenesSLC38A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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