A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001835



Internal ID6713969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77492849..77493574hg38UCSC Ensembl
Innerchr17:75488931..75489656hg19UCSC Ensembl
Innerchr17:73000526..73001251hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38726
hg19726
hg18726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586768
SamplesHuRef
Known GenesSEPT9
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001835
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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