A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398696



Internal ID21056249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1205201..1848200hg38UCSC Ensembl
chr6:1205436..1848434hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38643000
hg19642999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6043n223
Supporting Variantsnssv18214572
Samples
Known GenesFOXC1, FOXF2, FOXQ1, GMDS, MIR6720
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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