A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890914



Internal ID18838624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99393043..99409897hg38UCSC Ensembl
Outerchr6:99393043..99409897hg38UCSC Ensembl
Innerchr6:99840919..99857773hg19UCSC Ensembl
Outerchr6:99840919..99857773hg19UCSC Ensembl
Innerchr6:99947640..99964494hg18UCSC Ensembl
Outerchr6:99947640..99964494hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3816855
hg1916855
hg1816855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784603
Samples
Known GenesCOQ3, PNISR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890914
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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