A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892967



Internal ID19183787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15017680..15034194hg38UCSC Ensembl
Outerchr17:15017680..15034194hg38UCSC Ensembl
Innerchr17:14920997..14937511hg19UCSC Ensembl
Outerchr17:14920997..14937511hg19UCSC Ensembl
Innerchr17:14861722..14878236hg18UCSC Ensembl
Outerchr17:14861722..14878236hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3816515
hg1916515
hg1816515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781017
Samples
Known GenesCDRT7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892967
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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