A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586844



Internal ID7058226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63961483..63961950hg38UCSC Ensembl
Innerchr17:62038843..62039310hg19UCSC Ensembl
Innerchr17:59392575..59393042hg18UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38468
hg19468
hg18468
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv999259
Supporting Variants
SamplesHuRef
Known GenesSCN4A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586844
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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