A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635969



Internal ID7022766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27158052..27164686hg38UCSC Ensembl
Innerchr15:27158092..27164646hg38UCSC Ensembl
Outerchr15:27158012..27164726hg38UCSC Ensembl
chr15:27403199..27409833hg19UCSC Ensembl
Innerchr15:27403239..27409793hg19UCSC Ensembl
Outerchr15:27403159..27409873hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg386635
hg196635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15195317, essv15195316
SamplesNA10851, NA19758
Known GenesGABRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635969
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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