A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509508



Internal ID20882818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10016061..10034499hg38UCSC Ensembl
chr16:10109918..10128356hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3818439
hg1918439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028246
Samples
Known GenesGRIN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509508
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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