A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890807



Internal ID18838423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891931..29910087hg38UCSC Ensembl
Outerchr6:29883666..29913261hg38UCSC Ensembl
Innerchr6:29859708..29877864hg19UCSC Ensembl
Outerchr6:29851443..29881038hg19UCSC Ensembl
Innerchr6:29967687..29985843hg18UCSC Ensembl
Outerchr6:29959422..29989017hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3829596
hg1929596
hg1829596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780516, essv25797846, essv25781116, essv25796543, essv25782767
Samples
Known GenesHLA-H
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890807
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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