A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662546



Internal ID9928651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:154310366..154314291hg38UCSC Ensembl
Outerchr5:154310329..154314341hg38UCSC Ensembl
Innerchr5:153689926..153693851hg19UCSC Ensembl
Outerchr5:153689889..153693901hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg384013
hg194013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5739488
SamplesHG00183
Known GenesGALNT10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662546
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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