A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602855



Internal ID6989888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160027453..160035367hg38UCSC Ensembl
chr4:160948605..160956519hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg387915
hg197915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11662626, essv11662627, essv11662629, essv11662630, essv11662631, essv11662628
SamplesHG01465, HG00127, HG01383, HG03060, HG01468, HG01377
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602855
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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