A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501818



Internal ID20875055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26233601..26234900hg38UCSC Ensembl
chr16:26244922..26246221hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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