A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893068



Internal ID19183888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:7081725..7562319hg38UCSC Ensembl
Outerchr18:7080136..7564300hg38UCSC Ensembl
Innerchr18:7081724..7562317hg19UCSC Ensembl
Outerchr18:7080135..7564298hg19UCSC Ensembl
Innerchr18:7071724..7552317hg18UCSC Ensembl
Outerchr18:7070135..7554298hg18UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg38484165
hg19484164
hg18484164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790122, essv25788282, essv25788889, essv25791837, essv25788163, essv25792176, essv25788158
Samples
Known GenesLAMA1, LRRC30
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893068
Frequency
Sample Size3017
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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