A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514937



Internal ID20888292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4013248..4029706hg38UCSC Ensembl
chr16:4063249..4079707hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816459
hg1916459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030067
Samples
Known GenesADCY9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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