A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8935079



Internal ID13867793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28973616..28973634hg38UCSC Ensembl
Innerchr7:28973613..28973634hg38UCSC Ensembl
Outerchr7:28973595..28973655hg38UCSC Ensembl
chr7:29013232..29013250hg19UCSC Ensembl
Innerchr7:29013229..29013250hg19UCSC Ensembl
Outerchr7:29013211..29013271hg19UCSC Ensembl
chr7:28979757..28979775hg18UCSC Ensembl
Innerchr7:28979775..28979754hg18UCSC Ensembl
Outerchr7:28979736..28979796hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38278
hg19278
hg18278
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3373434
Supporting Variants
SamplesNA18517
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8935079
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