A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666461



Internal ID9585880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95128898..95130755hg38UCSC Ensembl
chr13:95781152..95783009hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6503147, essv5966741
SamplesNA18511, NA19350
Known GenesABCC4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666461
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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