A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677587



Internal ID9943692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10501216..10502107hg38UCSC Ensembl
Outerchr5:10501179..10502157hg38UCSC Ensembl
Innerchr5:10501328..10502219hg19UCSC Ensembl
Outerchr5:10501291..10502269hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5448555
SamplesHG01067
Known GenesLOC101929412
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677587
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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