A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663912



Internal ID9930017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41783902..41793380hg38UCSC Ensembl
chr15:42076100..42085578hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg389479
hg199479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6102719
SamplesNA19901
Known GenesMAPKBP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663912
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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