A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161456



Internal ID8252714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111181670..111518018hg38UCSC Ensembl
Innerchr7:110821726..111158074hg19UCSC Ensembl
Innerchr7:110608962..110945310hg18UCSC Ensembl
Innerchr7:110415677..110752025hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38336349
hg19336349
hg18336349
hg17336349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422497
Supporting Variants
SamplesND01675
Known GenesIMMP2L
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161456
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