A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662279



Internal ID9581698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34269976..34270362hg38UCSC Ensembl
chr15:34562177..34562563hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6112187, essv6524773, essv5544685
SamplesNA19359, NA18517, NA19190
Known GenesSLC12A6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662279
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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