A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603402



Internal ID20976473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144002001..144011300hg38UCSC Ensembl
chr6:144323138..144332437hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216928
Samples
Known GenesHYMAI, PLAGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603402
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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