A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893028



Internal ID19183848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51531920..51893363hg38UCSC Ensembl
Outerchr17:51531920..51893363hg38UCSC Ensembl
Innerchr17:49609281..49970723hg19UCSC Ensembl
Outerchr17:49609281..49970723hg19UCSC Ensembl
Innerchr17:46964280..47325722hg18UCSC Ensembl
Outerchr17:46964280..47325722hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38361444
hg19361443
hg18361443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788914
Samples
Known GenesCA10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893028
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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