A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501683



Internal ID20874920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50275315..50278442hg38UCSC Ensembl
chr16:50309226..50312353hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383128
hg193128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030005
Samples
Known GenesADCY7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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