A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890842



Internal ID18838458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35703874..35835415hg38UCSC Ensembl
Outerchr6:35678658..35837356hg38UCSC Ensembl
Innerchr6:35671651..35803192hg19UCSC Ensembl
Outerchr6:35646435..35805133hg19UCSC Ensembl
Innerchr6:35779629..35911170hg18UCSC Ensembl
Outerchr6:35754413..35913111hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38158699
hg19158699
hg18158699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787782, essv25788882
Samples
Known GenesARMC12, CLPS, CLPSL1, CLPSL2, FKBP5, LHFPL5, LOC285847, SRPK1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890842
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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