A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507206



Internal ID20880494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57676331..57679786hg38UCSC Ensembl
chr16:57710243..57713698hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383456
hg193456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029801
Samples
Known GenesGPR97
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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