A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499688



Internal ID20872911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9474714..9475380hg38UCSC Ensembl
chr16:9568571..9569237hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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