A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8936874



Internal ID14366691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108902913..108902935hg38UCSC Ensembl
Innerchr7:108902917..108902929hg38UCSC Ensembl
Outerchr7:108902895..108902953hg38UCSC Ensembl
chr7:108542970..108542992hg19UCSC Ensembl
Innerchr7:108542974..108542986hg19UCSC Ensembl
Outerchr7:108542952..108543010hg19UCSC Ensembl
chr7:108330206..108330228hg18UCSC Ensembl
Innerchr7:108330222..108330210hg18UCSC Ensembl
Outerchr7:108330188..108330246hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38281
hg19281
hg18281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3374712
Supporting Variants
SamplesNA18858
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8936874
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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