A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505545



Internal ID20878816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27903187..27919819hg38UCSC Ensembl
chr16:27914508..27931140hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3816633
hg1916633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029303
Samples
Known GenesGSG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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