A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5909544



Internal ID9154799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140882391..140888139hg38UCSC Ensembl
Outerchr7:140882354..140888189hg38UCSC Ensembl
Innerchr7:140582191..140587939hg19UCSC Ensembl
Outerchr7:140582154..140587989hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385836
hg195836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656982
Supporting Variants
SamplesHG01350
Known GenesBRAF
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5909544
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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