A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405108



Internal ID21062661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10387336..10583936hg38UCSC Ensembl
chr6:10387569..10584169hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38196601
hg19196601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216529
Samples
Known GenesGCNT2, LINC00518, MIR5689, TFAP2A, TFAP2A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405108
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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