A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635977



Internal ID7022774
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15195391, essv15195390
SamplesHG03718, HG03977
Known GenesGABRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635977
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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