A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008989



Internal ID19098207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107253038..107314723hg38UCSC Ensembl
Innerchr4:108174195..108235880hg19UCSC Ensembl
Innerchr4:108393644..108455329hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3861686
hg1961686
hg1861686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632589
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008989
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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