A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565557



Internal ID6690253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87726375..87727079hg38UCSC Ensembl
Outerchr16:87759981..87760685hg19UCSC Ensembl
Outerchr16:86317482..86318186hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38705
hg19705
hg18705
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006084
Supporting Variants
SamplesHuRef
Known GenesKLHDC4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565557
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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