A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411059



Internal ID21068612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28228275..28234509hg38UCSC Ensembl
chr6:28196053..28202287hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg386235
hg196235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140863
Samples
Known GenesZSCAN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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