A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499035



Internal ID20872251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19474272..19475662hg38UCSC Ensembl
chr16:19485594..19486984hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028153
Samples
Known GenesTMC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499035
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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