A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614286



Internal ID7001181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99925270..99936037hg38UCSC Ensembl
Innerchr7:99925476..99935831hg38UCSC Ensembl
Outerchr7:99925064..99936243hg38UCSC Ensembl
chr7:99522893..99533660hg19UCSC Ensembl
Innerchr7:99523099..99533454hg19UCSC Ensembl
Outerchr7:99522687..99533866hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810768
hg1910768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12908893, essv12908892, essv12908896, essv12908899, essv12908897, essv12908894, essv12908895, essv12908898
SamplesHG00640, HG04238, NA21116, HG03653, NA20849, HG04153, NA20908, HG04198
Known GenesGJC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614286
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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