A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893825



Internal ID19184645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176895386..176985584hg38UCSC Ensembl
Outerchr3:176895386..176985584hg38UCSC Ensembl
Innerchr3:176613174..176703372hg19UCSC Ensembl
Outerchr3:176613174..176703372hg19UCSC Ensembl
Innerchr3:178095868..178186066hg18UCSC Ensembl
Outerchr3:178095868..178186066hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3890199
hg1990199
hg1890199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791175
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893825
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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