A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656709



Internal ID9922814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85406374..85411008hg38UCSC Ensembl
chr15:85949605..85954239hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384635
hg194635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6517357, essv6120837, essv6262890, essv6393618, essv6269078, essv6135499, essv6455808, essv5829328, essv6163369, essv5931914, essv5959698, essv6567532
SamplesNA19381, NA18519, NA19917, NA19189, NA19437, NA19114, NA19225, NA19469, NA19256, NA19835, NA19467, NA18501
Known GenesAKAP13
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656709
Frequency
Sample Size1151
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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