A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893830



Internal ID19184650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:181132773..181167860hg38UCSC Ensembl
Outerchr3:181132773..181167860hg38UCSC Ensembl
Innerchr3:180850561..180885648hg19UCSC Ensembl
Outerchr3:180850561..180885648hg19UCSC Ensembl
Innerchr3:182333255..182368342hg18UCSC Ensembl
Outerchr3:182333255..182368342hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3835088
hg1935088
hg1835088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780937
Samples
Known GenesSOX2-OT
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893830
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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