A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891001



Internal ID19185397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170473308..170493087hg38UCSC Ensembl
Outerchr6:170463121..170493087hg38UCSC Ensembl
Innerchr6:170782396..170802175hg19UCSC Ensembl
Outerchr6:170772209..170802175hg19UCSC Ensembl
Innerchr6:170624321..170644100hg18UCSC Ensembl
Outerchr6:170614134..170644100hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3829967
hg1929967
hg1829967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797845, essv25797184, essv25796664, essv25796542, essv25796137, essv25796156, essv25796861, essv25796886, essv25796778
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891001
Frequency
Sample Size3017
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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