A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783754



Internal ID18817907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3512223..3972206hg38UCSC Ensembl
Innerchr3:3553907..4013890hg19UCSC Ensembl
Innerchr3:3528907..3988890hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38459984
hg19459984
hg18459984
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893637
Supporting Variants
Samples
Known GenesLRRN1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=154
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783754
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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