A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6085313



Internal ID9917470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5737175..5744586hg38UCSC Ensembl
Outerchr5:5737018..5744739hg38UCSC Ensembl
Innerchr5:5737288..5744699hg19UCSC Ensembl
Outerchr5:5737131..5744852hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg387722
hg197722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673815
Supporting Variants
SamplesNA20815
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6085313
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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