A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7751426



Internal ID13828714
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 StatusS
Merged Variantsesv3305380
Supporting Variants
SamplesNA18507
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7751426
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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