A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997696



Internal ID7081441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90000411..90006866hg38UCSC Ensembl
Outerchr15:90543643..90550098hg19UCSC Ensembl
Outerchr15:88344647..88351102hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386456
hg196456
hg186456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564635
SamplesHuRef
Known GenesZNF710
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997696
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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