A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596933



Internal ID6984247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88594403..88640746hg38UCSC Ensembl
chr3:88643553..88689896hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3846344
hg1946344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11067992
SamplesHG01048
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596933
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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