A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892983



Internal ID19183803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20056380..20088493hg38UCSC Ensembl
Outerchr17:20056380..20088493hg38UCSC Ensembl
Innerchr17:19959693..19991806hg19UCSC Ensembl
Outerchr17:19959693..19991806hg19UCSC Ensembl
Innerchr17:19900285..19932398hg18UCSC Ensembl
Outerchr17:19900285..19932398hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3832114
hg1932114
hg1832114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779518
Samples
Known GenesSPECC1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892983
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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