A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598213



Internal ID6985349
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11187884, essv11187883
SamplesHG03888, NA18579
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598213
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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