A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508728



Internal ID20882032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9223397..9264602hg38UCSC Ensembl
chr16:9317254..9358459hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3841206
hg1941206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179298
Samples
Known GenesMIR548X
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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