A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892445



Internal ID19183265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108157735..108184034hg38UCSC Ensembl
Outerchr13:108157735..108184034hg38UCSC Ensembl
Innerchr13:108810083..108836382hg19UCSC Ensembl
Outerchr13:108810083..108836382hg19UCSC Ensembl
Innerchr13:107608084..107634383hg18UCSC Ensembl
Outerchr13:107608084..107634383hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3826300
hg1926300
hg1826300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781328
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892445
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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