A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635970



Internal ID7022767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27224842..27226650hg38UCSC Ensembl
Innerchr15:27224846..27226646hg38UCSC Ensembl
Outerchr15:27224838..27226654hg38UCSC Ensembl
chr15:27469989..27471797hg19UCSC Ensembl
Innerchr15:27469993..27471793hg19UCSC Ensembl
Outerchr15:27469985..27471801hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15195323, essv15195324, essv15195326, essv15195321, essv15195329, essv15195318, essv15195320, essv15195319, essv15195325, essv15195322, essv15195327, essv15195328
SamplesNA19028, NA19190, HG02769, NA20291, HG03045, HG02882, NA19338, NA20296, HG02613, HG03433, HG01061, HG02760
Known GenesGABRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635970
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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