A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422405



Internal ID7906502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64249361..65171963hg38UCSC Ensembl
Innerchr7:63709739..64632341hg19UCSC Ensembl
Innerchr7:63347174..64269776hg18UCSC Ensembl
Innerchr7:63153889..64076491hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38922603
hg19922603
hg18922603
hg17922603
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161560
SamplesND02214
Known GenesCCT6P3, ERV3-1, LOC100128885, LOC641746, MIR6839, YWHAEP1, ZNF107, ZNF117, ZNF138, ZNF273, ZNF679, ZNF680, ZNF736
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422405
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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