A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600132



Internal ID6987176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32845400..32866466hg38UCSC Ensembl
chr4:32847022..32868088hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3821067
hg1921067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11388272
SamplesHG04161
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600132
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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