A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586149



Internal ID6710845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:7005907..7006407hg38UCSC Ensembl
Innerchr17:6909226..6909726hg19UCSC Ensembl
Innerchr17:6849950..6850450hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008363
Supporting Variants
SamplesHuRef
Known GenesALOX12, LOC100506713
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586149
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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