A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996092



Internal ID7080402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64340583..64341490hg38UCSC Ensembl
Outerchr15:64632782..64633689hg19UCSC Ensembl
Outerchr15:62419835..62420742hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38908
hg19908
hg18908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563465
SamplesHuRef
Known GenesCSNK1G1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996092
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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