A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11187883



Internal ID4351867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152744185..152776347hg38UCSC Ensembl
chr3:152461974..152494136hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3832163
hg1932163
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598213
Supporting Variants
SamplesHG03888
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11187883
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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