A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781221



Internal ID19171365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78354667..78453746hg38UCSC Ensembl
Innerchr6:79064384..79163463hg19UCSC Ensembl
Innerchr6:79121103..79220182hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3899080
hg1999080
hg1899080
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890889
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781221
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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