A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622184



Internal ID7009043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3984961..4014179hg38UCSC Ensembl
chr10:4027153..4056371hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3829219
hg1929219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13680542
SamplesHG03007
Known GenesMIR6078
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622184
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