A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892340



Internal ID19183160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46502430..46507977hg38UCSC Ensembl
Outerchr13:46502430..46507977hg38UCSC Ensembl
Innerchr13:47076565..47082112hg19UCSC Ensembl
Outerchr13:47076565..47082112hg19UCSC Ensembl
Innerchr13:45974566..45980113hg18UCSC Ensembl
Outerchr13:45974566..45980113hg18UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg385548
hg195548
hg185548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778864
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892340
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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