A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610251



Internal ID6997168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105075779..105139464hg38UCSC Ensembl
chr6:105523654..105587339hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3863686
hg1963686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12496765
SamplesNA11881
Known GenesBVES, BVES-AS1, LIN28B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610251
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer