A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597908



Internal ID6985046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137864610..137878792hg38UCSC Ensembl
chr3:137583452..137597634hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3814183
hg1914183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11159348, essv11159347, essv11159349
SamplesHG02070, HG02139, HG01807
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597908
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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