A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3361429



Internal ID15208407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69228533..69228577hg38UCSC Ensembl
Innerchr7:69228545..69228565hg38UCSC Ensembl
Outerchr7:69228521..69228589hg38UCSC Ensembl
chr7:68693520..68693564hg19UCSC Ensembl
Innerchr7:68693532..68693552hg19UCSC Ensembl
Outerchr7:68693508..68693576hg19UCSC Ensembl
chr7:68331456..68331500hg18UCSC Ensembl
Innerchr7:68331468..68331488hg18UCSC Ensembl
Outerchr7:68331444..68331512hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7864723, essv7864722, essv7864721
SamplesNA18871, NA18961, NA18522
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3361429
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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