A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599598



Internal ID6639862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10029051..10125617hg38UCSC Ensembl
chr4:10030675..10127241hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3896567
hg1996567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11352469
SamplesHG03965
Known GenesMIR3138, SLC2A9, WDR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599598
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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