A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890981



Internal ID18838691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162232577..162282387hg38UCSC Ensembl
Outerchr6:162221692..162288915hg38UCSC Ensembl
Innerchr6:162653609..162703419hg19UCSC Ensembl
Outerchr6:162642724..162709947hg19UCSC Ensembl
Innerchr6:162573599..162623409hg18UCSC Ensembl
Outerchr6:162562714..162629937hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3867224
hg1967224
hg1867224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797730, essv25799865
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890981
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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