A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893781



Internal ID19184601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146249386..146349953hg38UCSC Ensembl
Outerchr3:146249386..146349953hg38UCSC Ensembl
Innerchr3:145967173..146067740hg19UCSC Ensembl
Outerchr3:145967173..146067740hg19UCSC Ensembl
Innerchr3:147449863..147550430hg18UCSC Ensembl
Outerchr3:147449863..147550430hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38100568
hg19100568
hg18100568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800839, essv25786553
Samples
Known GenesPLSCR4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893781
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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