A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510004



Internal ID20883317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5322186..5985865hg38UCSC Ensembl
chr16:5372187..6035866hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38663680
hg19663680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180685
Samples
Known GenesMIR8065
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510004
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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