A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3357437



Internal ID15204416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37562941..37562953hg38UCSC Ensembl
Innerchr3:37562935..37562957hg38UCSC Ensembl
Outerchr3:37562923..37562971hg38UCSC Ensembl
chr3:37604432..37604444hg19UCSC Ensembl
Innerchr3:37604426..37604448hg19UCSC Ensembl
Outerchr3:37604414..37604462hg19UCSC Ensembl
chr3:37579436..37579448hg18UCSC Ensembl
Innerchr3:37579452..37579430hg18UCSC Ensembl
Outerchr3:37579418..37579466hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38287
hg19287
hg18287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8912802, essv8912794, essv8912808, essv8912813, essv8912799, essv8912806, essv8912798, essv8912810, essv8912809, essv8912812, essv8912811, essv8912815, essv8912800, essv8912801, essv8912804, essv8912805, essv8912807, essv8912796, essv8912797, essv8912795
SamplesNA11995, NA18561, NA18545, NA18526, NA18550, NA18960, NA18582, NA12828, NA18605, NA18537, NA18573, NA18555, NA18523, NA18576, NA18542, NA18909, NA12763, NA18552, NA12154, NA18577
Known GenesITGA9
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3357437
Frequency
Sample Size185
Observed Gain20
Observed Loss0
Observed Complex0
Frequencyn/a


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