A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676714



Internal ID9942819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56155744..56156712hg38UCSC Ensembl
chr15:56447942..56448910hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5719962, essv5516500, essv6461618, essv5546547, essv5500820, essv5576496
SamplesHG01140, NA19457, NA19137, HG01190, NA19712, NA19438
Known GenesRFX7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676714
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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