A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6112187



Internal ID9089590
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 StatusS
Merged Variantsesv2662279
Supporting Variants
SamplesNA19359
Known GenesSLC12A6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6112187
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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