A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15195317



Internal ID6231732
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635969
Supporting Variants
SamplesNA19758
Known GenesGABRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15195317
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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