A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893878



Internal ID19184698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4408687..4436196hg38UCSC Ensembl
Outerchr1:4408687..4436196hg38UCSC Ensembl
Innerchr1:4468747..4496256hg19UCSC Ensembl
Outerchr1:4468747..4496256hg19UCSC Ensembl
Innerchr1:4368607..4396116hg18UCSC Ensembl
Outerchr1:4368607..4396116hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3827510
hg1927510
hg1827510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797727
Samples
Known GenesLOC284661
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893878
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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