A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512972



Internal ID20886312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3196665..3208732hg38UCSC Ensembl
chr16:3246665..3258732hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3812068
hg1912068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028994
Samples
Known GenesOR1F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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