A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890801



Internal ID18838417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25274417..25428726hg38UCSC Ensembl
Outerchr6:25274417..25428726hg38UCSC Ensembl
Innerchr6:25274645..25428954hg19UCSC Ensembl
Outerchr6:25274645..25428954hg19UCSC Ensembl
Innerchr6:25382624..25536933hg18UCSC Ensembl
Outerchr6:25382624..25536933hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38154310
hg19154310
hg18154310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792910
Samples
Known GenesLRRC16A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890801
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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