A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15195391



Internal ID4476923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27489988..27491705hg38UCSC Ensembl
Innerchr15:27490005..27491689hg38UCSC Ensembl
Outerchr15:27489972..27491722hg38UCSC Ensembl
chr15:27735134..27736851hg19UCSC Ensembl
Innerchr15:27735151..27736835hg19UCSC Ensembl
Outerchr15:27735118..27736868hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381718
hg191718
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635977
Supporting Variants
SamplesHG03977
Known GenesGABRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15195391
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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