A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3303969



Internal ID15150917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156013065..156013066hg38UCSC Ensembl
Innerchr7:156013024..156013107hg38UCSC Ensembl
Outerchr7:156013023..156013108hg38UCSC Ensembl
chr7:155805759..155805760hg19UCSC Ensembl
Innerchr7:155805718..155805801hg19UCSC Ensembl
Outerchr7:155805717..155805802hg19UCSC Ensembl
chr7:155498520..155498521hg18UCSC Ensembl
Innerchr7:155498562..155498479hg18UCSC Ensembl
Outerchr7:155498478..155498563hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3876
hg1976
hg1876
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7741058, essv7755680, essv7759804, essv7747029, essv7742405
SamplesNA19172, NA18520, NA19114, NA19108, NA18517
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3303969
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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