A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661031



Internal ID9927136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:68109148..68110267hg38UCSC Ensembl
Outerchr5:68109111..68110317hg38UCSC Ensembl
Innerchr5:67404976..67406095hg19UCSC Ensembl
Outerchr5:67404939..67406145hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6579917
SamplesHG00154
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661031
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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