A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15195328



Internal ID6361934
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635970
Supporting Variants
SamplesNA20291
Known GenesGABRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15195328
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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