A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893081



Internal ID18837215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23843968..23913320hg38UCSC Ensembl
Outerchr1:23843968..23913320hg38UCSC Ensembl
Innerchr1:24170458..24239810hg19UCSC Ensembl
Outerchr1:24170458..24239810hg19UCSC Ensembl
Innerchr1:24043045..24112397hg18UCSC Ensembl
Outerchr1:24043045..24112397hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3869353
hg1969353
hg1869353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788296
Samples
Known GenesCNR2, FUCA1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893081
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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