A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892990



Internal ID19183810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:28988947..28998353hg38UCSC Ensembl
Outerchr17:28988947..28998353hg38UCSC Ensembl
Innerchr17:27315965..27325371hg19UCSC Ensembl
Outerchr17:27315965..27325371hg19UCSC Ensembl
Innerchr17:24340091..24349497hg18UCSC Ensembl
Outerchr17:24340091..24349497hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg389407
hg199407
hg189407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796416
Samples
Known GenesSEZ6
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892990
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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