A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514912



Internal ID20888267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67788201..67790000hg38UCSC Ensembl
chr16:67822104..67823903hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030832
Samples
Known GenesRANBP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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