A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780153



Internal ID19172942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89473670..89492658hg38UCSC Ensembl
Innerchr6:90183389..90202377hg19UCSC Ensembl
Innerchr6:90240108..90259096hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3818989
hg1918989
hg1818989
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890902
Supporting Variants
Samples
Known GenesANKRD6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780153
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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