A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656988



Internal ID9923093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178907579..178912124hg38UCSC Ensembl
Outerchr5:178907542..178912174hg38UCSC Ensembl
Innerchr5:178334580..178339125hg19UCSC Ensembl
Outerchr5:178334543..178339175hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384633
hg194633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6319321
SamplesNA18555
Known GenesZFP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656988
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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