A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986497



Internal ID12629160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161171068..161237312hg38UCSC Ensembl
Innerchr6:161592100..161658344hg19UCSC Ensembl
Innerchr6:161512090..161578334hg18UCSC Ensembl
Innerchr6:161562511..161628755hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3866245
hg1966245
hg1866245
hg1766245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752091
Supporting Variants
SamplesBEC_620
Known GenesAGPAT4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986497
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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