A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596979



Internal ID6984293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89881807..89887937hg38UCSC Ensembl
Innerchr3:89881857..89887887hg38UCSC Ensembl
Outerchr3:89881757..89887987hg38UCSC Ensembl
chr3:89930957..89937087hg19UCSC Ensembl
Innerchr3:89931007..89937037hg19UCSC Ensembl
Outerchr3:89930907..89937137hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg386131
hg196131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11069210, essv11069209
SamplesNA19315, NA18953
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596979
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer