A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15243415



Internal ID3879905
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636395
Supporting Variants
SamplesHG03520
Known GenesSEMA6D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15243415
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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