A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890948



Internal ID19185344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:191689020..191786782hg38UCSC Ensembl
Outerchr1:191677151..191788978hg38UCSC Ensembl
Innerchr1:191658150..191755912hg19UCSC Ensembl
Outerchr1:191646281..191758108hg19UCSC Ensembl
Innerchr1:189924773..190022535hg18UCSC Ensembl
Outerchr1:189912904..190024731hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38111828
hg19111828
hg18111828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797887, essv25786721, essv25796798
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890948
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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