A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514677



Internal ID20888032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58658584..58800395hg38UCSC Ensembl
chr16:58692488..58834299hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38141812
hg19141812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030874
Samples
Known GenesGOT2, SLC38A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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