A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659269



Internal ID9925374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7836786..7842087hg38UCSC Ensembl
chr5:7836899..7842200hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385302
hg195302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6211166
SamplesNA19147
Known GenesC5orf49
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659269
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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