A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892858



Internal ID19183678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2783827..2889542hg38UCSC Ensembl
Outerchr1:2783827..2961801hg38UCSC Ensembl
Innerchr1:2700372..2806107hg19UCSC Ensembl
Outerchr1:2700372..2878366hg19UCSC Ensembl
Innerchr1:2690232..2795967hg18UCSC Ensembl
Outerchr1:2690232..2868226hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38177975
hg19177995
hg18177995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788252, essv25788249
Samples
Known GenesTTC34
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892858
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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