A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497729



Internal ID20870937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22075699..22080695hg38UCSC Ensembl
chr16:22087020..22092016hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg384997
hg194997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028872
Samples
Known GenesC16orf52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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