A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010172



Internal ID7074237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47428436..47428609hg38UCSC Ensembl
chr15:47720633..47720806hg19UCSC Ensembl
chr15:45507925..45508098hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38174
hg19174
hg18174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3574510
SamplesHuRef
Known GenesSEMA6D
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010172
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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