A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3581380



Internal ID6706076
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 StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988489
Supporting Variants
SamplesHuRef
Known GenesNUBP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3581380
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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