A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510265



Internal ID20883582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10815158..10826965hg38UCSC Ensembl
chr16:10909015..10920822hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3811808
hg1911808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028304
Samples
Known GenesTVP23A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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