A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6102719



Internal ID9803605
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 Flag1
Merged StatusS
Merged Variantsesv2663912
Supporting Variants
SamplesNA19901
Known GenesMAPKBP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6102719
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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