A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3308017



Internal ID14808279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77351446..77351447hg38UCSC Ensembl
Innerchr7:77351419..77351474hg38UCSC Ensembl
Outerchr7:77351418..77351475hg38UCSC Ensembl
chr7:76980763..76980764hg19UCSC Ensembl
Innerchr7:76980736..76980791hg19UCSC Ensembl
Outerchr7:76980735..76980792hg19UCSC Ensembl
chr7:76818699..76818700hg18UCSC Ensembl
Innerchr7:76818727..76818672hg18UCSC Ensembl
Outerchr7:76818671..76818728hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38197
hg19197
hg18197
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7836678
SamplesNA19239
Known GenesGSAP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3308017
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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