A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636395



Internal ID7023189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47541055..47548551hg38UCSC Ensembl
Innerchr15:47541055..47548551hg38UCSC Ensembl
Outerchr15:47540797..47548806hg38UCSC Ensembl
chr15:47833252..47840748hg19UCSC Ensembl
Innerchr15:47833252..47840748hg19UCSC Ensembl
Outerchr15:47832994..47841003hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg387497
hg197497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15243414, essv15243413, essv15243415
SamplesHG03520, HG03159, HG02580
Known GenesSEMA6D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636395
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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