A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3412585



Internal ID15259544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155890797..155892195hg38UCSC Ensembl
Innerchr7:155891195..155891797hg38UCSC Ensembl
Outerchr7:155889797..155893195hg38UCSC Ensembl
chr7:155683491..155684889hg19UCSC Ensembl
Innerchr7:155683889..155684491hg19UCSC Ensembl
Outerchr7:155682491..155685889hg19UCSC Ensembl
chr7:155376252..155377650hg18UCSC Ensembl
Innerchr7:155377252..155376650hg18UCSC Ensembl
Outerchr7:155375252..155378650hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695663
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3412585
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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