A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636804



Internal ID6676911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68387073..68398737hg38UCSC Ensembl
Innerchr15:68387073..68398737hg38UCSC Ensembl
Outerchr15:68386573..68399237hg38UCSC Ensembl
chr15:68679412..68691076hg19UCSC Ensembl
Innerchr15:68679412..68691076hg19UCSC Ensembl
Outerchr15:68678912..68691576hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3811665
hg1911665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15279454
SamplesHG03779
Known GenesITGA11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636804
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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