A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890796



Internal ID19185098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21207319..21228657hg38UCSC Ensembl
Outerchr6:21207319..21228657hg38UCSC Ensembl
Innerchr6:21207550..21228888hg19UCSC Ensembl
Outerchr6:21207550..21228888hg19UCSC Ensembl
Innerchr6:21315529..21336867hg18UCSC Ensembl
Outerchr6:21315529..21336867hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3821339
hg1921339
hg1821339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798439, essv25801198
Samples
Known GenesCDKAL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890796
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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