A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512440



Internal ID20885774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19185389..19187150hg38UCSC Ensembl
chr16:19196711..19198472hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381762
hg191762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028133
Samples
Known GenesSYT17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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