A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505747



Internal ID20879020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8442619..8494377hg38UCSC Ensembl
chr16:8492621..8544379hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3851759
hg1951759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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