A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514113



Internal ID20887465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2794859..2796523hg38UCSC Ensembl
chr16:2844860..2846524hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381665
hg191665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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