A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890991



Internal ID18838701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162587986..162629816hg38UCSC Ensembl
Outerchr6:162587986..162629816hg38UCSC Ensembl
Innerchr6:163009018..163050848hg19UCSC Ensembl
Outerchr6:163009018..163050848hg19UCSC Ensembl
Innerchr6:162929008..162970838hg18UCSC Ensembl
Outerchr6:162929008..162970838hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3841831
hg1941831
hg1841831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784814
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890991
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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