A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891785



Internal ID18839495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37054668..37554529hg38UCSC Ensembl
Outerchr10:37034858..37573196hg38UCSC Ensembl
Innerchr10:37343596..37843457hg19UCSC Ensembl
Outerchr10:37323786..37862124hg19UCSC Ensembl
Innerchr10:37383602..37883463hg18UCSC Ensembl
Outerchr10:37363792..37902130hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38538339
hg19538339
hg18538339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790510, essv25788216
Samples
Known GenesANKRD30A, LINC00993
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891785
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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