A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000463



Internal ID6712607
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587138
SamplesHuRef
Known GenesNPY5R
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000463
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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