A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890916



Internal ID19185312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100611010..100630842hg38UCSC Ensembl
Outerchr6:100591339..100637070hg38UCSC Ensembl
Innerchr6:101058886..101078718hg19UCSC Ensembl
Outerchr6:101039215..101084946hg19UCSC Ensembl
Innerchr6:101165607..101185439hg18UCSC Ensembl
Outerchr6:101145936..101191667hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3845732
hg1945732
hg1845732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785560, essv25785666, essv25784592
Samples
Known GenesASCC3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890916
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer