A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587138



Internal ID6711834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:163345703..163346154hg38UCSC Ensembl
Innerchr4:164266855..164267306hg19UCSC Ensembl
Innerchr4:164486305..164486756hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38452
hg19452
hg18452
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000463
Supporting Variants
SamplesHuRef
Known GenesNPY5R
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587138
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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