A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596913



Internal ID6984227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88106223..88197093hg38UCSC Ensembl
chr3:88155373..88246243hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3890871
hg1990871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11066219
SamplesHG02236
Known GenesC3orf38, CGGBP1, ZNF654
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596913
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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