A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1504476



Internal ID5634580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89122127..89122264hg38UCSC Ensembl
chr16:89188535..89188672hg19UCSC Ensembl
chr16:87716036..87716173hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38138
hg19138
hg18138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4204969
SamplesHuRef
Known GenesACSF3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1504476
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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