A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893772



Internal ID19184592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:125143841..125157913hg38UCSC Ensembl
Outerchr3:125143841..125157913hg38UCSC Ensembl
Innerchr3:124862685..124876757hg19UCSC Ensembl
Outerchr3:124862685..124876757hg19UCSC Ensembl
Innerchr3:126345375..126359447hg18UCSC Ensembl
Outerchr3:126345375..126359447hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3814073
hg1914073
hg1814073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778417
Samples
Known GenesMIR5092, SLC12A8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893772
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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