A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3577162



Internal ID6701858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13198219..13198296hg38UCSC Ensembl
chr16:13292076..13292153hg19UCSC Ensembl
chr16:13199577..13199654hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3878
hg1978
hg1878
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009468
Supporting Variants
SamplesHuRef
Known GenesSHISA9
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3577162
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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