A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3374712



Internal ID15221687
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 StatusM
Merged Variants
Supporting Variantsessv8936875, essv8936871, essv8936874, essv8936877, essv8936870, essv8936876, essv8936868, essv8936872, essv8936873
SamplesNA18861, NA18510, NA19138, NA18520, NA18523, NA18858, NA19147, NA19116, NA19129
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3374712
Frequency
Sample Size185
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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