A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511322



Internal ID20884649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56607750..56611308hg38UCSC Ensembl
chr16:56641662..56645220hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg383559
hg193559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189668
Samples
Known GenesMT2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511322
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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