A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596915



Internal ID6984229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88155868..88168209hg38UCSC Ensembl
chr3:88205018..88217359hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3812342
hg1912342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11066223, essv11066222, essv11066221
SamplesHG02583, HG02582, HG02236
Known GenesC3orf38
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596915
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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