A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596446



Internal ID6983761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66978257..66988333hg38UCSC Ensembl
Innerchr3:66978257..66988333hg38UCSC Ensembl
Outerchr3:66977757..66988833hg38UCSC Ensembl
chr3:67028681..67038757hg19UCSC Ensembl
Innerchr3:67028681..67038757hg19UCSC Ensembl
Outerchr3:67028181..67039257hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3810077
hg1910077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11030917, essv11030916
SamplesHG00106, HG03920
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596446
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