A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893051



Internal ID18837185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81244320..81272804hg38UCSC Ensembl
Outerchr17:81244320..81272804hg38UCSC Ensembl
Innerchr17:79218120..79246604hg19UCSC Ensembl
Outerchr17:79218120..79246604hg19UCSC Ensembl
Innerchr17:76832715..76861199hg18UCSC Ensembl
Outerchr17:76832715..76861199hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3828485
hg1928485
hg1828485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787988
Samples
Known GenesSLC38A10
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893051
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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