A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995232



Internal ID6731182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15775408..15775457hg38UCSC Ensembl
chr16:15869265..15869314hg19UCSC Ensembl
chr16:15776766..15776815hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3577535
SamplesHuRef
Known GenesMYH11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995232
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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