A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890980



Internal ID18838690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162176920..162318733hg38UCSC Ensembl
Outerchr6:162163721..162329393hg38UCSC Ensembl
Innerchr6:162597952..162739765hg19UCSC Ensembl
Outerchr6:162584753..162750425hg19UCSC Ensembl
Innerchr6:162517942..162659755hg18UCSC Ensembl
Outerchr6:162504743..162670415hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38165673
hg19165673
hg18165673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779043, essv25780612, essv25781252, essv25798764, essv25784217, essv25783750, essv25799890, essv25797762, essv25796150, essv25797753
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890980
Frequency
Sample Size3017
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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