A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3347161



Internal ID15194143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97217793..97217812hg38UCSC Ensembl
Innerchr7:97217789..97217816hg38UCSC Ensembl
Outerchr7:97217770..97217835hg38UCSC Ensembl
chr7:96847105..96847124hg19UCSC Ensembl
Innerchr7:96847101..96847128hg19UCSC Ensembl
Outerchr7:96847082..96847147hg19UCSC Ensembl
chr7:96685041..96685060hg18UCSC Ensembl
Innerchr7:96685064..96685037hg18UCSC Ensembl
Outerchr7:96685018..96685083hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9635258
SamplesNA11918
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3347161
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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