A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409275



Internal ID21066828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41595312..41596627hg38UCSC Ensembl
chr6:41563050..41564365hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143332
Samples
Known GenesFOXP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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