A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007713



Internal ID7072808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169245563..169284233hg38UCSC Ensembl
Innerchr1:169214801..169253471hg19UCSC Ensembl
Innerchr1:167481425..167520095hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3838671
hg1938671
hg1838671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586048
SamplesHuRef
Known GenesNME7
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007713
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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