A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997367



Internal ID7081337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50109929..50145357hg38UCSC Ensembl
Innerchr5:49405763..49441191hg19UCSC Ensembl
Innerchr5:49441520..49476948hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3835429
hg1935429
hg1835429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586230
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997367
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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