A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890976



Internal ID19185372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160819809..160833648hg38UCSC Ensembl
Outerchr6:160810560..160836386hg38UCSC Ensembl
Innerchr6:161240841..161254680hg19UCSC Ensembl
Outerchr6:161231592..161257418hg19UCSC Ensembl
Innerchr6:161160831..161174670hg18UCSC Ensembl
Outerchr6:161151582..161177408hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3825827
hg1925827
hg1825827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787142, essv25800219, essv25800176
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890976
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