A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988489



Internal ID6724460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10764756..10764861hg38UCSC Ensembl
chr16:10858613..10858718hg19UCSC Ensembl
chr16:10766114..10766219hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38106
hg19106
hg18106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3581380
SamplesHuRef
Known GenesNUBP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988489
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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