A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509271



Internal ID20882580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12082593..12117572hg38UCSC Ensembl
chr16:12176450..12211429hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3834980
hg1934980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028678
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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