A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497052



Internal ID20870256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9382525..9384667hg38UCSC Ensembl
chr16:9476382..9478524hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg382143
hg192143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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