A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511705



Internal ID20885035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30017689..30019050hg38UCSC Ensembl
chr16:30029010..30030371hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381362
hg191362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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