A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398501



Internal ID21056054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1466398..1647557hg38UCSC Ensembl
chr6:1466633..1647791hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38181160
hg19181159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217061
Samples
Known GenesFOXC1, GMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398501
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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