A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3305380



Internal ID15152328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95635466..95635467hg38UCSC Ensembl
Innerchr7:95635436..95635497hg38UCSC Ensembl
Outerchr7:95635435..95635498hg38UCSC Ensembl
chr7:95264778..95264779hg19UCSC Ensembl
Innerchr7:95264748..95264809hg19UCSC Ensembl
Outerchr7:95264747..95264810hg19UCSC Ensembl
chr7:95102714..95102715hg18UCSC Ensembl
Innerchr7:95102745..95102684hg18UCSC Ensembl
Outerchr7:95102683..95102746hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38217
hg19217
hg18217
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7741039, essv7744745, essv7761328, essv7760232, essv7751426, essv7763089, essv7747201
SamplesNA18507, NA19190, NA18907, NA19114, NA18499, NA18517, NA18501
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3305380
Frequency
Sample Size185
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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