A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497154



Internal ID20870359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57661882..57662696hg38UCSC Ensembl
chr16:57695794..57696608hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029800
Samples
Known GenesGPR56
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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