A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890803



Internal ID18838419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27771601..27814760hg38UCSC Ensembl
Outerchr6:27771601..27814760hg38UCSC Ensembl
Innerchr6:27739380..27782538hg19UCSC Ensembl
Outerchr6:27739380..27782538hg19UCSC Ensembl
Innerchr6:27847359..27890517hg18UCSC Ensembl
Outerchr6:27847359..27890517hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3843160
hg1943159
hg1843159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778794
Samples
Known GenesHIST1H2AI, HIST1H2AJ, HIST1H2BL, HIST1H3H
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890803
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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