A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892580



Internal ID19183400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103205897..103230167hg38UCSC Ensembl
Outerchr14:103201980..103241080hg38UCSC Ensembl
Innerchr14:103672234..103696504hg19UCSC Ensembl
Outerchr14:103668317..103707417hg19UCSC Ensembl
Innerchr14:102741987..102766257hg18UCSC Ensembl
Outerchr14:102738070..102777170hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3839101
hg1939101
hg1839101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784287, essv25784509, essv25800656, essv25799713, essv25797750, essv25797498, essv25801163
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892580
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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