A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161565



Internal ID7906279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144253455..144410494hg38UCSC Ensembl
Innerchr6:144574591..144731630hg19UCSC Ensembl
Innerchr6:144616284..144773323hg18UCSC Ensembl
Innerchr6:144616284..144773323hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38157040
hg19157040
hg18157040
hg17157040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422260
Supporting Variants
SamplesND05165
Known GenesUTRN
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161565
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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