A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780937



Internal ID19175388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:181132773..181167860hg38UCSC Ensembl
Innerchr3:180850561..180885648hg19UCSC Ensembl
Innerchr3:182333255..182368342hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3835088
hg1935088
hg1835088
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893830
Supporting Variants
Samples
Known GenesSOX2-OT
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780937
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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