A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029585



Internal ID19118803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:49550951..49614179hg38UCSC Ensembl
Innerchr7:49590547..49653775hg19UCSC Ensembl
Innerchr7:49561093..49624321hg18UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3863229
hg1963229
hg1863229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661261
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)nsv1029585
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